Pestana Chap 4 - General Surgery Flashcards

1
Q

When the diagnosis of GERD is uncertain, what test should be done?

A

pH monitoring is best to establish the presence of reflux and its correlation with the symptoms

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2
Q

What is the typical case of GERD?

A

An overweight individual that complains of burning retrosternal pain and “heartburn” that is brought about by bending over, wearing tight clothing, or lying flat in bed at night; and relieved by the ingestion of antacids or OTC H2 blockers

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3
Q

What is the concern with longstanding GERD?

A

The concern is the damage that might have been done to the lower esophagus (peptic esophagitis) and the possible development of Barrett esophagus

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4
Q

What is the indicated test for longstanding GERD?

A

Indicated tests:

1) Endoscopy
2) Biopsies

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5
Q

When is surgery appropriate for GERD? When is surgery necessary for GERD? When is surgery imperative for GERD?

A

Surgery for GERD:

1) Is appropriate for longstanding symptomatic disease that cannot be controlled by medical means
2) Is necessary in anyone who has developed complications (ulceration, stenosis)
3) Is imperative if there are severe dysplastic changes

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6
Q

What is the usual surgical procedure for GERD? How is it performed? What should be added to Nissen if severe dysplastic changes are present?

A

1) Laparoscopic Nissen fundoplication
2) In a fundoplication, the gastric fundus (upper part) of the stomach is wrapped, or plicated, all the way 360 degrees around the lower end of the esophagus and stitched in place, reinforcing the closing function of the lower esophageal sphincter. The esophageal hiatus is also narrowed down by sutures to prevent or treat concurrent hiatal hernia, in which the fundus slides up through the enlarged esophageal hiatus of the diaphragm
3) Radiofrequency ablation should be added to Nissen if severe dysplastic changes are present

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7
Q

What are two common recognizable clinical patterns found with esophageal motility problems?

A

1) Crushing pain with swallowing in uncoordinated massive contraction
2) Suggestive pattern of dysphagia seen in achalasia, where solids are swallowed with less difficulty than liquids

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8
Q

What is the first test done for an esophageal motility problem? What is the test for definitive diagnosis?

A

1) Barium swallow is typically done first

2) Manometry studies are used for the definitive diagnosis

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9
Q

Is achalasia more common in men or in women?

A

Achalsia is seen more commonly in women

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10
Q

What are common clinical pearls of achalasia?

A

1) There is dysphagia that is worse for liquids
2) The patient eventually learns that sitting up straight and waiting allows the weight of the column of liquid to overcome the sphincter
3) There is occasional regurgitation of undigested food

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11
Q

In a patient with achalasia, what will be seen on X-rays?

A

Megaesophagus

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12
Q

What is the diagnostic test for achalasia?

A

Manometry is diagnostic

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13
Q

What is the most appealing current treatment for achalasia?

A

The most appealing current treatment is balloon dilitation done by endoscopy

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14
Q

What is the classic clinical presentation of cancer of the esophagus?

A

1) There is a classic progression of dysphagia starting with meat, then other solids, then soft foods, eventually liquids, and finally (in several months) saliva
2) Significant weight loss is always seen

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15
Q

Who most commonly develops squamous cell carcinoma of the esophagus?

A

Squamous cell carcinoma of the esophagus is seen in men with a history of smoking and drinking (blacks have high incidence)

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16
Q

Who most commonly develops adenocarcinoma of the esophagus?

A

Adenocarcinoma of the esophagus is seen in people with long-standing gastroesophageal reflux

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17
Q

What diagnostic test establishes the diagnosis of cancer of the esophagus? What must precede this test to help prevent inadvertent perforation of the esophagus?

A

Diagnosis for both squamous cell and adenocarcinoma of the esophagus is established with endoscopy and biopsies, but barium swallow must precede the endoscopy to help prevent inadvertent perforation

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18
Q

What is the function of performing a CT scan in patients with esophageal cancer? What is the function of surgery in esophageal cancer?

A

1) CT scan assesses operability of the esophagus

2) Most cases can only get palliative (rather than curative) surgery

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19
Q

When does a Mallory-Weiss tear occur? What is a sign of a Mallory-Weiss tear?

A

1) Mallory-Weiss tear occurs after prolonged, forceful vomiting
2) Eventually, bright red blood comes up

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20
Q

How is a Mallory-Weiss tear diagnosed? How is it treated?

A

Endoscopy establishes diagnosis and allows photocoagulation (laser)

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21
Q

How does Boerhaave syndrome begin? What is the clinical presentation of Boerhaave syndrome?

A

1) Boerhaave syndrome starts with prolonged, forceful vomiting leading to esophageal perforation
2) There is continuous, severe, wrenching epigastric and low sternal pain of sudden onset, soon followed by fever, leukocytosis, and a very sick-looking patient

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22
Q

How is diagnosis of Boerhaave made? How is it treated?

A

1) Contrast swallow (Gastrografin first, barium if negative) is diagnostic
2) Emergency surgical repair should follow
3) Delay in diagnosis and treatment has grave consequences

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23
Q

What is the most common reason for esophageal perforation?

A

Instrumental perforation of the esophagus is by far the most common reason for esophageal perforation

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24
Q

How does intrumental perforation of the esophagus present? How is it treated?

A

1) Shortly after completion of endoscopy, symptoms as described for Boerhaave syndrome (continuous, severe, wrenching epigastric and low sternal pain of sudden onset, soon followed by fever, leukocytosis, and a very sick-looking patient) will develop. There may be emphysema in the lower neck (virtually diagnostic in this setting)
2) Contrast studies and prompt repair are imperative

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25
Q

In what age group is gastric adenocarcinoma more common?

A

Gastric adenocarcinoma is more common in the elderly

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26
Q

What is the common presentation of gastric adenocarcinoma?

A

There is anorexia, weight loss, and vague epigastric distress or early satiety. Ocassionally there is hematemesis

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27
Q

How is gastric adenocarcinoma diagnosed? What is the function of CT scan in gastric adenocarcinoma? What is the best therapy?

A

1) Endoscopy and biopsies are diagnostic
2) CT scan helps assess operability
3) Surgery is the best therapy

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28
Q

How common is gastric lymphoma in relation to gastric adenocarcinoma and how does it present?

A

1) Gastric lymphoma is nowadays almost as common as gastric adenocarcinoma
2) Presentation and diagnosis are similar (There is anorexia, weight loss, and vague epigastric distress or early satiety. Ocassionally there is hematemesis)

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29
Q

What is the treatment for gastric lymphoma? How can low-grade lymphomatoid transformation (Maltoma) be reversed?

A

1) Treatment is based on chemotherapy or radiotherapy
2) Surgery is done if perforation is feared as the tumor melts away
3) Low-grade lymphomatoid transformation (Maltoma) can be reversed by eradication of H.pylori

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30
Q

What is the typical cause of mechanical intestinal obstruction? How does it present? What can be heard on auscultation early on?

A

1) Mechanical intestinal obstruction is typically caused by adhesions in those who have had a prior laparotomy
2) There is colicky abdominal pain and protracted vomiting, progressive abdominal distention (if it is a low obstruction), and no passage of gas or feces
3) Early on, high-pitched bowel sounds coincide with the colicky pain (after a few days there is silence)

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31
Q

What do X-rays of a mechanical intestinal obstruction show?

A

X-rays show distended loops of small bowel, with air-fluid levels

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32
Q

How is mechanical intestinal obstruction treated?

A

1) Treatment starts with NPO, NG suction, and IV fluids, hoping for spontaneous resolution, while watching for early signs of strangulation
2) Surgery is done if conservative management is unsuccessful, within 24 hours in cases of complete obstruction or within a few days in cases of partial obstruction

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33
Q

How does a strangulated obstruction present? How is it treated?

A

1) Strangulated obstruction (compromised blood supply) starts as a mechanical intestinal obstruction does (There is colicky abdominal pain and protracted vomiting, progressive abdominal distention (if it is a low obstruction), and no passage of gas or feces), but eventually the patient develops fever, leukocytosis, constant pain, signs of peritoneal irritation, and ultimately full-blown peritonitis and sepsis
2) Emergency surgery is required

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34
Q

How does mechanical intestinal obstruction caused by an incarcerated hernia present? How is it treated?

A

1) Mechanical intestinal obstruction caused by an incarcerated hernia presents with colicky abdominal pain and protracted vomiting, progressive abdominal distention (if it is a low obstruction), and no passage of gas or feces, but can eventually lead to strangulation in which the patient develops fever, leukocytosis, constant pain, signs of peritoneal irritation, and ultimately full-blown peritonitis and sepsis
2) Physical exam however, shows the irreducible hernia that used to be reducible
3) Because we can effectively eliminate the hernia (we cannot effectively eliminate adhesions), all of these undergo surgical repair, but the timing varies: emergently after proper rehydration in those who appear to be strangulated; electively in those who can be reduced manually and have viable bowel

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35
Q

Which patients present with carcinoid syndrome? How does this syndrome present?

A

1) Carcinoid syndrome is seen in patients with a small bowel carcinoid tumor with liver metastasis
2) The syndrome includes diarrhea, flushing of the face, wheezing, and right-sided heart valvular damage (look for prominent jugular venous pulse)

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36
Q

How is carcinoid syndrome diagnosed?

A

24-hour urinary collection for 5-hydroxyindoleacetic acid provides the diagnosis. (Hint: Whenever syndromes produce episodic attacks or spells, the offending agent will be at high concentrations in the blood only at the time of the attack. A blood sample taken afterward will be normal. Thus, a 24-hour urinary collection is more likely to provide the diagnosis)

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37
Q

What is the classic picture of acute appendicitis? What is found on physical exam and labs? What is the treatment?

A

1) The classic picture of acute appendicitis begins with anorexia, followed by vague periumbilical pain that several hours later becomes sharp, severe, constant, and localized to the right lower quadrant of the abdomen
2) Tenderness, guarding, and rebound are found to the right and below the umbilicus (not elsewhere in the belly)
3) There is modest fever and leukocytosis in the 10,000-15,000 range, with neutrophilia and immature forms
4) Emergency appendectomy should follow

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38
Q

How do doubtful presentations of acute appendicitis present? How are they diagnosed?

A

1) Doubtful presentations that could be acute appendicitis include any that do not have all the classic findings
2) CT scan has become the standard diagnostic modality for those cases

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39
Q

How does cancer of the right colon present? In what age group does it present? Is there occult blood? What tests are diagnostic? What is the treatment of choice?

A

1) Cancer of the right colon typically shows up with anemia (hypochromic, iron deficiency) in the right age group (elderly), for no good reason
2) Stools will be 4+ for occult blood
3) Colonoscopy and biopsies are diagnostic
4) Surgery (right hemicolectomy) is treatment of choice

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40
Q

How does cancer of the left colon present? What are the first diagnostic studies done? What needs to be done before surgical treatment? What is the function of CT scan in cancer of the left colon?

A

1) Cancer of the left colon typically shows with bloody bowel movements. Blood coats the outside of the stool, there may be constipation, and stools may have narrow caliber
2) Flexible proctosigmoidoscopic exam (45 or 60 cm) and biopsies are usually the first diagnostic study
3) Before surgery is done, full colonoscopy is needed to rule out synchronous second primary. Pre-op chemotherapy and radiation may be needed for large rectal cancers
4) CT scan helps assess operability and extent

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41
Q

Can colonic polyps be premalignant? If so, what is the descending order of probability for malignant degeneration? Which polyps are not premalignant?

A

1) Yes, colonic polyps may be premalignant
2) In descending order of probability for malignant degeneration are familial polyposis (and variants such as Gardner), familial multiple inflammatory polyps, villous adenoma, and adenomatous polyp
3) Poylps that are not premalignant include juvenile, Peutz-Jeghers, isolated inflammatory, and hyperplastic

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42
Q

What kind of diarrhea do Crohn’s disease and chronic ulcerative colitis (CUC) produce? When is Crohn’s disease treated surgically? When is CUC treated surgically?

A

1) Crohn’s disease and CUC produce severe diarrhea with blood and mucus
2) Crohn’s disease and CUC can happen in multiple GI locations, and thus cannot be cured by surgical resection. Crohn’s disease is surgically treated only when there are complications such as bleeding, stricture, or fistulization
3) CUC can be surgically cured but is avoided because it always requires removal of the rectal mucosa, raising the need for a stoma or an ileoanal anastomosis. Indications for surgery in CUC include active disease for more than 20 years (malignant degeneration), severe nutritional depletion, multiple hospitalizations, need for high-dose steroids or immunosuppressants, or development of toxic megacolon (fever, leukocytosis, abdominal pain and tenderness, and massively dilated colon with gas within the wall)

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43
Q

How is pseudomembranous enterocolitis caused? What are symptoms? How is the diagnosis best made? What is the treatment of choice?

A

1) Pseudomembranous enterocolitis is caused by overgrowth of Clostridium difficile in patients who have been on antibiotics. Any antibiotic can do it. Clindamycin was the first one described, and, currently, cephalosporins are the most common cause
2) There is profuse, watery diarrhea, crampy abdominal pain, fever, and leukocytosis
3) The diagnosis is best made by identifying the toxin in the stool. Stool cultures take too long, and the pseudomembranes are not always seen on endoscopy. The culpable antibiotic should be discontinued, and no antidiarrheals should be used
4) Metronidazole is the treatment of choice, with vancomycin serving as an alternate. A virulent form of the disease, unresponsive to treatment, with a WBC above 50,000 and serum lactate above 5, requires emergency colectomy

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44
Q

What is a recently reported effective cure for the overgrowth of C. diff?

A

Fecal enema has been recently reported as a very effective cure for the overgrowth of C. diff. It makes sense that restoring normal bowel flora would help in this situation

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45
Q

What should be ruled out in all anorectal disease and how is it done?

A

In all anorectal disease cancer should be ruled out by proper physical exam (including proctosigmoidoscopic exam), even though the clinical presentation may suggest a specific benign process

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46
Q

Which type of hemorrhoid bleeds? Which type is painful?

A

1) Hemorrhoids typically bleed when they are internal (can be treated with rubber band ligation), or hurt when they are external may need surgery if conservative treatment fails)
2) Internal hemorrhoids can become painful and produce itching if they are prolapsed

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47
Q

Who commonly develops an anal fissure? How does it present? What is believed to cause and perpetuate the problem? What is the choice of therapy?

A

1) Anal fissures happen to young women
2) They have exquisite pain with defecation and blood streaks covering the stools. The fear of pain is so intense that they avoid bowel movements (and get constipated) and sometimes refuse proper physical examination of the area. Exam may need to be done under anesthesia (the fissure is usually posterior, in the midline)
3) A tight sphincter is believed to cause and perpetuate the problem, thus therapy is directed at relaxing it: stool softeners, topical nitroglycerin, local injection of botulinum toxin, forceful diltation or lateral internal sphincterotomy
4) Calcium channel blockers such as diltiazem ointment 2% TID topically for 6 weeks have had an 80-90% success rate, as compared to only 50% success for botulinum toxin

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48
Q

How does anorectal Crohn’s disease present? How is it treated?

A

1) Crohn’s disease often affects the anal area. It starts with a fissure, fistula, or small ulceration, but the diagnosis should be suspected when the area fails to heal and gets worse after surgical interventions (the anal area typically heals very well because it has excellent blood supply-failure to do so means Crohn’s disease)
2) Surgery, in fact, should not be done in Crohn’s disease of the anus. A fistula, if present, could be drained with setons while medical therapy is underway. Remicade (infliximab) helps healing

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49
Q

How does an ischiorectal (perirectal) abscess present?

A

1) Ischiorectal abscess (perirectal abscess) is very common
2) Patient is febrile, with exquisite perirectal pain that does not let him sit down or have bowel movements
3) Physical exam shows all the classic findings of an abscess (rubor, dolor, calor, and tumor) lateral to the anus, between the rectum and the ischial tuberosity

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50
Q

How is a ischiorectal (perirectal) abscess treated and what should be ruled out during the procedure? What should one look out for after treatment if the patient is severely diabetic?

A

1) Incision and drainage are needed, and cancer should be ruled out by proper examination during the procedure
2) If a patient is severely diabetic, horrible necrotizing soft tissue infection may follow: watch him closely

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51
Q

How can a fistula-in-ano form?

A

1) Fistula-in-ano develops in some patients who have had an ischiorectal abscess drained
2) Epithelial migration from the anal crypts (where the abscess originated) and from the perineal skin (where the drainage was done) form a permanent tract

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52
Q

What do patients complain of with a fistula-in-ano? What does physical exam show?

A

1) Patient reports fecal soiling and occasional perineal discomfort
2) Physical exam shows opening (or openings) lateral to the anus, a cordlike tract may be felt, and discharge may be expressed

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53
Q

What should you rule out when a fistula-in-ano may be present? How is a fistula-in-ano treated?

A

1) Rule out necrotic and draining tumor

2) Treat with fistulotomy

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54
Q

Who more commonly develops squamous cell carcinoma of the anus?

A

Squamous cell carcinoma of the anus is more common in HIV+, and in homosexuals with receptive sexual practices

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55
Q

How does squamous cell carcinoma of the anus present? What additional finding can be palpated on physical exam commonly?

A

1) A fungating mass grows out of the anus

2) Metastatic inguinal nodes are often felt

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56
Q

How is squamous cell carcinoma of the anus diagnosed? How is it treated?

A

1) Diagnose with biopsy
2) Treatment starts with Nigro chemoradiation protocol, followed by surgery if there is residual tumor
3) Currently the 5-week chemo-radiation protocol has a 90% success rate, so surgery rarely is required

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57
Q

What is Nigro chemoradiation protocol?

A

Nigro protocol is the pre-operative use of chemotherapy with 5-fluorouracil and mitomycin and medical radiation for squamous cell carcinomas of the anal canal of less than 5 cm, followed by surgical excision if necessary

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58
Q

Where do most GI bleeds originate from? Where do the remaining GI bleeds originate from?

A

1) General statistics of GI bleeding show that 3 of 4 cases originate in the upper GI tract (from the tip of the nose to the ligament of Treitz)
2) 1 of 4 originates in the colon or rectum, and very few arise from the jejunum of ileum

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59
Q

What are causes of GI bleeding arising from the colon? Where are GI bleeds most commonly seen in younger patients as compared to older patients?

A

1) GI bleeding arising from the colon comes from angiodysplasia, polyps, diverticulosis, or cancer, all of which are diseases of old people. Even hemorrhoids become more common with age
2) Thus, when a young patient has GI bleeding, the odds are overwhelming that is comes from the upper GI tract. When an old patient bleeds, it could be from anywhere (an “equal opportunity bleeder”), as the upper GI is the most common source overall (3/4), but age makes that old patient a good candidate for lower GI bleeding. Statistics are helpful when the bleeding is per rectum, but they are not needed when patients vomit blood

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60
Q

When a patient vomits blood, where does it originate from? What about when blood is recovered by NG tube? If blood is recovered from an NG tube, what is the next best diagnostic test? What should you first check before conducting this diagnostic test?

A

1) Vomiting blood always denotes a source within the upper GI (tip of the nose to the ligament of Treitz)
2) The same is true when blood is recovered by NG tube in a patient who shows up with bleeding per rectum
3) The best next diagnostic test in that setting is upper GI endoscopy
4) Be sure to look at the mouth and nose first

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61
Q

What does melena (black, tarry stools) indicate? How should you begin workup for melena?

A

1) Melena always indicates digested blood, thus it must originate high enough to undergo digestion
2) Start workup with upper GI endoscopy

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62
Q

Where does red blood per rectum originate from? What series of steps should first be done to determine if the origin of actively bleeding red blood per rectum is from an upper GI bleed?

A

1) Red blood per rectum could come from anywhere in the GI tract (including upper GI, as it may have transited too fast to be digested)
2) The first diagnostic maneuver if the patient is actively bleeding at the time is to pass an NG tube and aspirate gastric contents. If blood is retrieved, an upper source has been established (follow with upper endoscopy). If no blood is retrieved and the fluid is white (no bile), the territory from the tip of the nose to the pylorus has been excluded, but the duodenum is still a potential source. Upper GI endoscopy should follow. If no blood is recovered and the fluid is green (bile tinged), the entire upper GI (tip of the nose to the ligament of Treitz) has been excluded, and there is no need for an upper GI endoscopy

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63
Q

When upper GI bleed has been excluded, how should active bleeding per rectum be worked up?

A

1) Active bleeding per rectum, when upper GI has been excluded, is more difficult to work up
2) Bleeding hemorrhoids should always be excluded first (anoscopy), but colonoscopy is not helpful during active bleeding (the oncoming blood obscures the field)
3) There are two ways to go after the hemorrhoids have been excluded. Some practitioners proceed according to the estimated rate of bleeding. If it exceeds 2 mL/min (1 unit of blood every 4 hours), they do an angiogram, which has a very good chance of finding the source and may allow for angiographic embolization. If the bleeding is less than 0.5 mL/min, they wait until the bleeding stops and then do a colonoscopy. For the cases in-between, they may do a tagged red-cell study. If the tagged blood puddles somewhere, an angiogram may be productive. The curse of the tagged red cell study is that it is a slow test. By the time it’s finished, the patient is often no longer bleeding, and the subsequent angiogram is useless. In that case, at least there is some idea if the puddling is on the right or the left and could thus guide a potential “blind” hemicolectomy in the future. If the tagged red cells do not show up on the scan, a subsequent colonoscopy is planned. Some practitioners always begin with the tagged red-cell study, regardless of the estimated rate of bleeding
4) With increasing frequency in clinical practice, when bleeding is not found to be in the colon, capsule endoscopy is done to localize the spot in the small bowel, once the patient is stable.

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64
Q

How should workup be started for a patient with a recent history of blood per rectum, but no active bleeding at the time of presentation?

A

Patients with a recent history of blood per rectum, but not actively bleeding at the time of presentation, should start workup with upper GI endoscopy if they are young (overwhelming odds); but if they are old they need both an upper and a lower GI endoscopy (at the same session)

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65
Q

What is the most common cause of blood per rectum in a child? How should you start the work up of this condition?

A

1) Blood per rectum in a child should be from Meckel diverticulum
2) Start workup with technetium scan, looking for the ectopic gastric mucosa

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66
Q

What is the most likely cause of massive upper GI bleeding in the stressed, multiple trauma, or complicated post-op patient?

A

Stress ulcers

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67
Q

What are stress ulcers? Where are they found?

A

1) A stress ulcer is a single or multiple mucosal defect which can become complicated by upper gastrointestinal bleeding during the physiologic stress of serious illness
2) Ordinary peptic ulcers are found commonly in the gastric antrum and the duodenum whereas stress ulcers are found commonly in fundic mucosa and can be located anywhere within the stomach and proximal duodenum

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68
Q

How do you confirm the diagnosis of a suspected stress ulcer?

A

Endoscopy

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69
Q

What is the best therapeutic option for a stress ulcer? How can a stress ulcer be avoided?

A

1) Angiographic embolization

2) Stress ulcers should be avoided by maintaining the gastric pH above 4

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70
Q

What are categorical processes that can cause acute abdominal pain?

A

1) Perforation
2) Obstruction
3) Inflammatory or ischemic processes

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71
Q

How does acute abdominal pain caused by perforation present? What is the confirmatory diagnosis?

A

1) Acute abdominal pain caused by perforation has sudden onset and is constant, generalized, and very severe
2) The patient is reluctant to move, and very protective of his abdomen
3) Except in the very old or very sick, impressive generalized signs of peritoneal irritation are found (tenderness, muscle guarding, rebound, silent abdomen)
4) If present, free air under the diaphragm in upright x-rays confirms the diagnosis

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72
Q

What is the most common example of acute abdominal pain caused by perforation? What is the treatment of acute abdominal pain caused by perforation?

A

1) Perforated peptic ulcer is the most common example

2) Emergency surgery is needed

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73
Q

How does acute abdominal pain caused by obstruction of a duct (ureter, cystic, or common) present?

A

1) Acute abdominal pain caused by obstruction of a narrow duct (ureter, cystic, or common) has sudden onset of very severe colicky pain, with typical location and radiation according to source
2) The patient moves constantly, seeking a position of comfort
3) There are few physical findings, and they are limited to the area where the process is

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74
Q

How does acute abdominal pain caused by inflammatory process present? What are the physical exam and lab findings?

A

1) Acute abdominal pain caused by inflammatory process has gradual onset and slow buildup (at the very least a couple of hours, more commonly 6 or 10 or 12 hours), it is constant, starts as ill-defined, eventually locates to the area where the problem is, and often has typical radiation patterns
2) There are physical findings of peritoneal irritation in the affected area, and (except for pancreatitis) systemic signs such as fever and leukocytosis

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75
Q

What is a characteristic feature of ischemic processes of acute abdominal pain?

A

Ischemic processes affecting the bowel are the only ones that combine severe abdominal pain with blood in the lumen of the gut

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76
Q

When should primary peritonitis be suspected in a patient? What will cultures of the ascitic fluid reveal? How is primary peritonitis treated?

A

1) Primary peritonitis should be suspected in the child with nephrosis and ascites, or the adult with ascites who has a “mild” generalized acute abdomen with equivocal physical findings, and perhaps some fever and leukocytosis
2) Cultures of the ascitic fluid will yield a single organism (in garden-variety acute abdomens, a multiplicity of organisms grow)
3) Treat with antibiotics, not with surgery

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77
Q

What is the treatment for a generalized acute abdomen? What conditions that mimic a generalized acute abdomen should be ruled out before treatment and what tests can be done to rule these conditions out?

A

1) The treatment for a generalized acute abdomen is exploratory laparotomy, with no need to have a specific diagnosis as to the exact nature of the process
2) If it does not look like primary peritonitis (one of the exceptions), we only need to rule out things that may mimic an acute abdomen-myocardial ischemia (EKG, tropnins), lower lobe pneumonia (chest x-ray), PE (immobilized patient)-or things that specifically do not require surgery-pancreatitis (amylase or lipase) and urinary stones (CT scan of abdomen)

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78
Q

When should acute pancreatitis be most suspected? What is the classic picture of acute pancreatitis?

A

1) Acute pancreatitis should be suspected in the alcoholic who develops an “upper” acute abdomen
2) The classic picture has rapid onset for an inflammatory process (a couple of hours), and the pain is constant, epigastric, radiating straight through to the back, with nausea, vomiting, and retching
3) Physical findings are relatively modest, found in the upper abdomen

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79
Q

How is acute pancreatitis diagnosed? What if the diagnosis is unclear?

A

1) Diagnose with serum or urinary amylase or lipase (serum from 12 to 48 hours, urinary from third to sixth day)
2) CT if diagnosis is unclear

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80
Q

How is acute pancreatitis treated?

A

Treat with NPO, NG suction, IV fluids

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81
Q

In what patients should biliary tract disease be suspected?

A

Biliary tract disease should be suspected in the fat woman in her forties who has “fifty-five children,” and who develops right upper quadrant abdominal pain

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82
Q

How do ureteral stones present? What will be found on urinalysis? What is the best diagnostic test?

A

1) Ureteral stones produce sudden onset of colicky flank pain radiating to inner thigh and scrotum (or labia), sometimes with other urinary symptoms like urgency and frequency; and with microhematuria in the urinalysis
2) CT scan is the best diagnostic test

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83
Q

What is one of the very few inflammatory processes giving acute abdominal pain in the left lower quadrant? What is the common age group for the this condition? What is the common presentation for this condition?

A

1) Acute diverticulitis is one of the very few inflammatory processes giving acute abdominal pain in the left lower quadrant (in women the tube and ovary are other potential sources)
2) Patient is middle-age or beyond
3) There is fever, leukocytosis, physical findings of peritoneal irritation in the left lower quadrant, and sometimes a palpable tender mass

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84
Q

What is the diagnostic test for acute diverticulitis? How is it first treated? If initial treatment does not work, what is the next treatment option? In the presence of an abscess, what can be done? Who is eligible for elective surgery?

A

1) CT is diagnostic
2) Start treatment with NPO, IV fluids, antibiotics. Most will cool down
3) Emergency surgery is needed for those who do not
4) Radiologically guided percutaneous drainage of abscess may precede resection
5) Elective surgery for those who have had at least two or more attacks

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85
Q

Volvulus of the sigmoid is commonly seen in what age group? What are two clinical signs of volvulus of the sigmoid?

A

1) Old people

2) Intestinal obstruction and severe abdominal distention

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86
Q

What is the diagnostic test for volvulus of the sigmoid? How can it be treated? What is recommended for recurrent cases?

A

1) X-rays are diagnostic, as they show air-fluid levels in the small bowel, very distended colon, and a huge air-filled loop in the right upper quadrant that tapers down toward the left lower quadrant with the shape of a “parrot’s beak”
2) Proctosigmoidoscopic exam with the old rigid instrument resolves the acute problem. Rectal tube is left in
3) Recurrent cases need elective sigmoid resection

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87
Q

Mesenteric ischemia is commonly seen in what age group? What is the real key to development of mesenteric ischemia?

A

1) Mesenteric ischemia is seen predominantly in the elderly
2) The real key is the development of an acute abdomen in someone with atrial fibrillation or a recent MI (the source of the clot that breaks off and lodges in the superior mesenteric artery)

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88
Q

Why is the diagnosis of mesenteric ischemia often made late? What diagnostic test may save the day in a very early case of mesenteric ischemia?

A

1) Because the very old do not mount impressive acute abdomens, often the diagnosis is made late, when there is blood in the bowel lumen (the only condition that mixes acute pain with GI bleeding) and acidosis and sepsis have developed
2) In very early cases, arteriogram and embolectomy might save the day

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89
Q

In the United States, primary hepatoma (hepatocellular carcinoma) is only seen in patients with what conditions?

A

Primary hepatoma (hepatocellular carcinoma) is seen in the United States only in people with cirrhosis, or those known to have had hepatitis B or C

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90
Q

How does primary hepatoma present? What is the specific blood marker? What test will show the location and extent of the hepatoma? What treatment can be done if possible?

A

1) Patients develop vague right upper-quadrant discomfort and weight loss
2) The specific blood marker is alpha-fetoprotein
3) CT scan will show location and extent
4) Resection is done if technically possible

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91
Q

Is there more metastatic or primary cancer of the liver? How much more?

A

Metastatic cancer of the liver outnumbers primary cancer of the liver in the United States by 20:1

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92
Q

How is metastatic cancer of the liver found?

A

They are found by CT scan if follow-up for the treated primary tumor is under way, or suspected because of rising carcinoembryonic antigen (CEA) in those who had colonic cancer

93
Q

How is metastatic cancer of the liver typically treated? What is another way to control the cancer?

A

1) If the primary is slow growing and the metastases are confined to one lobe, resection can be done
2) Other means of control include radioablation

94
Q

How do hepatic adenomas arise? Why are they important to identify?

A

1) Hepatic adenomas may arise as a complication of birth control pills
2) They are important because they have a tendency to rupture and bleed massively inside the abdomen

95
Q

What is the diagnostic test for hepatic adenoma? How is it treated?

A

1) CT scan is diagnostic

2) Emergency surgery is required

96
Q

Pyogenic liver abscess is often a complication of what condition? How do patients present?

A

1) Pyogenic liver abscess is seen most often as a complication of biliary tract disease, particularly acute ascending cholangitis
2) Patients develop fever, leukocytosis, and a tender liver

97
Q

How is a pyogenic liver abscess diagnosed? How is it treated?

A

1) Sonogram or CT scan are diagnostic

2) Percutaneous drainage is required

98
Q

Who most often develops amebic abscess of the liver? How does an amebic abscess of the liver present?

A

1) Amebic abscess of the liver favors men, all of whom have a “Mexico connection.” (It is very common there and seen here in immigrants)
2) It presents very similarly to a pyogenic liver abscess (Patients develop fever, leukocytosis, and a tender liver)

99
Q

How is an amebic abscess of the liver diagnosed? How is it treated?

A

1) Definitive diagnosis is given by serology (the ameba does not grow in the pus)
2) Because the serological diagnostic test takes weeks to be reported, empiric treatment is started in those clinically suspected. The treatment is generally metronidazole, seldom requiring drainage. If they improve, it is continued-if not, drainage is done

100
Q

What are three classifications of jaundice?

A

1) Hemolytic
2) Hepatocellular
3) Obstructive

101
Q

How elevated is the bilirubin in a hemolytic jaundice? What type of bilirubin is elevated? Is there any bile in the urine? What should workup determine?

A

1) Hemolytic jaundice is usually low level (bilirubin of 6 or 8, but not 35 or 40)
2) All the elevated bilirubin is unconjugated (indirect), with no elevation of the direct, conjugated fraction
3) There is no bile in the urine
4) Workup should determine what is chewing up the red cells

102
Q

What labs are typically elevated in hepatocellular jaundice? What is the most common example of a cause of hepatocellular jaundice?

A

1) Hepatocellular jaundice has elevation of both fractions of bilirubin and very high levels of transaminases, with modest elevation of alkaline phosphatase
2) Hepatitis is the most common example, and workup should proceed in that direction (serologies to determine specific type)

103
Q

What labs are typically elevated in obstructive jaundice? What is the first step in your workup of obstructive jaundice?

A

1) Obstructive jaundice has elevations of both fractions of bilirubin, modest elevation of transaminases, and very high levels of alkaline phosphatase
2) First step in the workup is a sonogram, looking for dilatation of the biliary ducts, as well as further clues as to the nature of the obstructive process

104
Q

In obstructive jaundice caused by stones, where are stones commonly seen? In malignant obstruction, what structure will often be identified and what is this sign called?

A

1) In obstruction caused by stones, the stone that is obstructing the common duct is seldom seen, but stones are seen in the gallbladder, which because of chronic irritation cannot dilate
2) In malignant obstruction, a large, thin-walled, distended gallbladder is often identified (Courvoisier-Terrier sign)

105
Q

In who should we suspect obstructive jaundice caused by stones? What specific lab will be elevated? What will be seen on ultrasound?

A

Obstructive jaundice caused by stones should be suspected in the obese, fecund woman in her forties who has high alkaline phosphatase, dilated ducts on sonogram, and nondilated gallbladder full of stones

106
Q

What should be done if obstructive jaundice is suspected?

A

The next move is to endoscopic retrograde cholangiopancreatography (ERCP) to confirm the diagnosis, do sphincterotomy, and remove the common duct stone. Cholecystectomy should follow

107
Q

What is an ERCP? How is it done? How long does it usually take

A

1) An endoscopic retrograde cholangiopancreatogram (ERCP) is an invasive procedure that allows visualization and instrumentation of the biliary and pancreatic ducts
2) An endoscope descends into the duodenum, the ampulla is cannulated, and x-ray dye is injected
3) Although experts can do the ERCP in less than an hour, the need for sedation makes ERCP an all-day affair: nothing by mouth for several hours prior to the test; then the procedure itself; perhaps a bit of discomfort (gagging) if the sedation is light; and then a recovery period, after which the patient needs a ride home

108
Q

What is an MRCP?

A

1) A newer study, magnetic resonance cholangiopancreatogram (MRCP) is completely noninvasive and is done on a fully awake patient
2) Every now and then it’s necessary to hold breathing for about 10 seconds at a time, and the whole thing is over in roughly 10 minutes. No gagging, no limitations, Simple. And the pictures thus produced are gorgeous: detailed views of both ducts and the surrounding parenchyma

109
Q

When should you choose an ERCP vs a MRCP?

A

1) Obviously, if all you need is a diagnostic picture, the clear choice is MRCP. But if you want to do more than look at a picture, you will need the ERCP. With the latter you can do sphincerotomies, retrieve stones, drain pus, deploy stents, biopsy tumors, and so on. Introduced as a diagnostic study only, ERCP has evolved into an instrument for therapy-which MRCP cannot do
2) Sometimes a progressive sequence will make sense: Get your diagnosis and make your plans with the 10-minute, noninvasive test (MRCP). They, if the findings call for manipulations, schedule the all-day affair (ERCP)

110
Q

When is obstructive jaundice caused by tumor suggested? What are the different cancers that may be responsible?

A

1) Obstructive jaundice caused by tumor is suggested by the thin-walled, dilated gallbladder in the sonogram
2) The different cancers that may be responsible are adenocarcinoma of the head of the pancreas, adenocarcinoma of the ampulla of Vater, or cholangiocarcinoma of the common duct itself

111
Q

In the presence of obstructive jaundice caused by tumor, what signs/symptoms are suggestive of a large pancreatic tumor? How should the tumor be diagnosed? What if symptoms are negative or if a CT scan is negative?

A

1) Significant weight loss and constant back pain suggest a large pancreatic tumor, which should be visible in a CT scan-the next test to run
2) In the absence of those clues or if the CT scan is negative, the next step is MRCP, which can show smaller tumors that are blocking the flow of bile thanks to strategic location-a cholangiocarcinoma, an ampullary cancer, or a small pancreatic malignancy abutting the intrapancreatic portion of the common duct

112
Q

What options are available for a biopsy of a tumor causing obstructive jaundice?

A

1) CT-guided percutaneous for a large pancreatic mass
2) Endoscopic for ampullary
3) ERCP and brushings for a ductal neoplasm
4) Endoscopic ultrasound for tiny tumors within the head of the pancreas

113
Q

When are ampullary cancers suspected as a cause of obstructive jaundice? What test should be done first for diagnosis and why?

A

1) Ampullary cancers may be suspected when malignant obstructive jaundice coincides with anemia and positive blood in the stools
2) Ampullary cancer can bleed into the lumen like any other mucosal malignancy, at the same time that it can obstruct biliary flow by virtue of its location. Given that combination, endoscopy should be the first test

114
Q

Is pancreatic cancer usually cured? Do ampullary cancer and cancer of the lower end of the common duct have a better prognosis?

A

1) Pancreatic cancer is seldom cured, even when the huge Whipple operation (pancreatoduodenectomy) is done
2) Ampullary cancer and cancer of the lower end of the common duct have a much better prognosis (about 40% cure)

115
Q

When do cholangiocarcinomas in a certain location have terrible prognosis? Can a margin-free resection commonly be done?

A

1) Cholangiocarcinomas that arise within the liver at the bifurcation of the hepatic ducts have terrible prognosis by virtue of their extremely inconvenient location
2) They can be beautifully shown by magnetic resonance cholangiopancreatography (MRCP), but achieving margin-free resection is almost impossible

116
Q

What is responsible for the vast majority of biliary tract pathology? Who commonly develops this condition?

A

1) Gallstones
2) Although the obese woman in her forties is the “textbook” victim, incidence increases with age so that eventually they are common in everybody, particularly Mexican Americans and Native

117
Q

How are asymptomatic gallstones treated?

A

Asymptomatic gallstones are left alone

118
Q

When does biliary colic occur? How does it present?

A

1) Biliary colic occurs when a stone temporarily occludes the cystic duct
2) There is colicky pain in the right upper quadrant, radiating to the right shoulder and beltlike to the back, often triggered by ingestion of fatty food, accompanied by nausea and vomiting but without signs of peritoneal irritation or systemic signs of inflammatory process

119
Q

How long does an episode of biliary colic usually last if untreated? How can it be treated? How are gallstones diagnosed? What is biliary colic cured?

A

1) The episode is self-limited (10, 20, maybe 30 minutes) or easily aborted by anticholinergics
2) Sonogram establishes diagnosis of gallstones
3) Elective cholecystectomy if sonogram is establishes the diagnosis

120
Q

What pathophysiology differentiates biliary colic from acute cholecystitis? What differs on physical exam and labs?

A

1) Acute cholecystitis starts as a biliary colic, but the stone remains at the cystic duct until an inflammatory process develops in the obstructed gallbladder
2) Pain becomes constant, there is modest fever and leukocytosis, and there are physical findings of peritoneal irritation in the right upper quadrant
3) Liver function tests are minimally affected

121
Q

What is the diagnostic test for acute cholecystitis? If this test is negative and acute cholecystitis is still suspected, what other test should be done?

A

1) Sonogram is diagnostic in most cases (gallstones, thick-walled gallbladder, and pericholecystic fluid)
2) Rarely, a radionuclide scan (HIDA) might be needed (would show uptake in the liver, common duct, and duodenum, but not in the occluded gallbladder)

122
Q

What is the initial treatment of acute cholecystitis?

A

NG suction, NPO, IV fluids, and antibiotics “cool down” most cases, allowing elective cholecystectomy to follow

123
Q

When is cholecystectomy usually done on a patient with acute cholecystitis? When is it emergent? What is the best treatment option if a patient is very ill, but has prohibitive surgical risk?

A

1) Physicians typically endeavor to do cholecystectomy in the same hospital admission, as an urgent case, though it is not a “middle of the night” true emergency
2) If the patient does not respond (men and diabetics often do not), emergency cholecystectomy is needed
3) Emergency percutaneous transhepatic cholecystostomy may be the best temporizing option in the very sick with prohibitive surgical risk

124
Q

What is acute ascending cholangitis?

A

Acute ascending cholangitis is a far more deadly disease than acute cholecystitis, in which stones have reached the common duct producing partial obstruction and ascending infection

125
Q

Are patients with acute ascending cholangitis usually younger or older? Are they sicker than patients with acute cholecystitis? What is acute ascending cholangitis?

A

1) Patients are often older and sicker
2) Acute ascending cholangitis is a far more deadly disease, in which stones have reached the common duct producing partial obstruction and ascending infection

126
Q

What findings indicate sepsis for acute ascending cholangitis?

A

Temperature spikes to 104-105F, with chills, and very high white blood cell (WBC) count

127
Q

What is the key lab finding for acute ascending cholangitis? What is an additional lab finding that is present?

A

1) Extremely high levels of alkaline phosphatase

2) There is some hyperbilirubinemia

128
Q

What are lifesaving therapies for acute ascending cholangitis? What procedure must follows?

A

1) IV antibiotics & Emergency decompression of the common duct (ideally by ERCP, alternatively percutaneous through the liver by percutaneous transhepatic cholangiogram [PTC], or rarely by surgery)
2) Eventually cholecystectomy has to follow

129
Q

What is the pathophysiology of biliary pancreatitis?

A

Biliary pancreatitis is seen when stones become impacted distally in the ampulla, temporarily obstructing both pancreatic and biliary ducts

130
Q

What is the fate of the stones in biliary pancreatitis? What labs are elevated? What test confirms the diagnosis in the presence of these labs and symptoms?

A

1) The stones often pass spontaneously, producing a mild and transitory episode of cholangitis along with the classic manifestations of pancreatitis (elevated amylase or lipase)
2) Sonogram confirms gallstones in the gallbladder

131
Q

How is biliary pancreatitis treated conservatively? What happens if conservative treatment fails?

A

1) Conservative treatment (NPO, NG suction, IV fluids) usually leads to improvement, allowing elective cholecystectomy to be done later
2) If not, ERCP and sphincterotomy may be required to dislodge the impacted stone

132
Q

Acute pancreatitis is typically a complication of what two things?

A

1) Gallstones

2) Alcoholism

133
Q

What are the different classifications of acute pancreatitis?

A

1) Edematous
2) Hemorrhagic
3) Suppurative (pancreatic abscess)

134
Q

What are two late complications of acute pancreatitis?

A

1) Pancreatic pseudocyst

2) Chronic pancreatitis

135
Q

In which patients does acute edematous pancreatitis usually occur in? How does it present?

A

1) Alcoholics or in patients with gallstones
2) Epigastric and midabdominal pain starts after a heavy meal or bout of alcoholic intake, is constant, radiates straight through to the back, and is accompanied by nausea, vomiting and (after the stomach is empty) continued retching

136
Q

For a patient with acute edematous pancreatitis, what finding is found on physical exam? What elevated lab values are diagnostic? How does resolution occur?

A

1) There is tenderness and mild rebound in the upper abdomen
2) Elevated serum amylase or lipase (early on) or urinary amylase or lipase (after a couple of days) are diagnostic, and a key finding to establish the edematous nature is an elevated hematocrit
3) Resolution usually follows a few days of pancreatic rest (NPO, NG suction, IV fluids)

137
Q

How does acute hemorrhagic pancreatitis differ from acute edematous pancreatitis? What are some other initial characteristic parts of acute hemorrhagic pancreatitis? What about the next morning?

A

1) Acute hemorrhagic pancreatitis is a much more deadly disease. It starts as the edematous form does, but an early laboratory clue is lower hematocrit (the degree of amylase elevation does not correlate with the severity of the disease)
2) Other findings have been catalogued (Ranson’s criteria), and they include at the time of presentation elevated WBC count, elevated blood glucose, and low serum calcium
3) By the next morning, the hematocrit is even lower, the serum calcium remains low (in spite of calcium administration), the blood urea nitrogen (BUN) goes up, and metabolic acidosis and low arterial PO2 eventually are evident

138
Q

Once acute hemorrhagic pancreatitis progresses, what is the treatment option?

A

Prognosis at that time is bad, and very intensive supportive therapy is needed (in the ICU)

139
Q

What is the final common pathway for death in acute hemorrhagic pancreatitis and what can be done about this?

A

1) A common final pathway for death is the development of multiple pancreatic abscesses
2) Try to anticipate them and drain them, if at all possible
3) Daily CT scans are recommended

140
Q

What antibiotic can be used by physicians in patients with signs of infected pancreatitis?

A

Intravenous imipenem (or meropenem in those with a seizure disorder) is used by some physicians in patients with signs of infected pancreatitis

141
Q

How does a pancreatic abscess come to surgical attention? How is it treated?

A

1) Pancreatic abscesses come to surgical attention via imaging studies, or when fever and leukocytosis develop about 10 days after the onset of pancreatitis
2) Ideally percutaneous radiological drainage should be performed. Because that is not always possible, open drainage may be required

142
Q

What is the best way to deal with necrotic pancreas? When is it best to do this procedure? How is this procedure done?

A

1) Necrosectomy
2) This operation is best done when the dead tissue is well delineated, typically after 4 weeks
3) The material is “scooped out” and may have to be repeated until all the dead matter has been cleared away

143
Q

What is pancreatic pseudocyst a complication of? When does it usually arise? What is the classic presentation?

A

1) Pancreatic pseudocyst can be a late sequela of acute pancreatitis or of pancreatic (upper abdominal) trauma
2) In either case about 5 weeks elapses between the original problem and the discovery of the pseudocyst
3) There is a collection of pancreatic juice outside the pancreatic ducts (most commonly in the lesser sac) and the pressure symptoms thereof (early satiety, vague discomfrot, a deep palpable mass)

144
Q

What test is diagnostic of pancreatic pseudocyst? What determines whether or not the pseudocyst requires treatment? What is the treatment?

A

1) CT or sonogram will be diagnostic
2) Treatment is dictated by the size and age of the pseudocyst. Cysts 6 cm or smaller, or those that have been present for less than 6 weeks are not likely to have complications and can be observed for spontaneous resolution. Bigger (>6 cm) or older cysts (>6 wk) are more likely to rupture or bleed, and they need to be treated
3) Treatment involved drainage of the cyst. The cyst can be drained percutaneously to the outside, drained surgically into the gastrointestinal tract, or drained endoscopically into the stomach

145
Q

What develops in patients with repeated episodes of chronic pancreatitis?

A

People who have repeated episodes of pancreatitis (usually alcoholic) eventually develop calcified burned-out pancreas, steatorrhea, diabetes, and constant epigastric pain, which is why chronic pancreatitis is a devastating disease

146
Q

What part of chronic pancreatitis is manageable and what part is usually not?

A

The diabetes and steatorrhea can be controlled with insulin and pancreatic enzymes, but the pain is resistant to most modalities of therapy and it wrecks sufferers’ lives

147
Q

What can be done to help chronic pancreatitis if MRCP shows specific points of obstruction and dilatation?

A

Operations that drain the pancreatic duct may help

148
Q

Why should all abdominal hernias be electively repaired? What are exceptions to this? When is abdominal hernia repair emergent?

A

1) All abdominal hernias should be electively repaired to avoid the risk of intestinal obstruction and strangulation
2) Exceptions include umbilical hernias in patients younger than 2 to 5 years of age (they may close by themselves) and esophageal sliding (para-esophageal) hiatal hernias (which are not “true” hernias)
3) Hernias that become irreducible need emergency surgery to prevent strangulation. Those that have been irreducible for years need elective repair only

149
Q

What are the 3 big families of malignant tumors?

A

There are 3 big families of malignant tumors, which arise from the 3 layers of the embryo:

1) Epithelial tumors, which come from the ectoderm
2) Sarcomas, which originate in mesodermal tissue
3) Adenocarcinomas, which grow from the endoderm

150
Q

What makes a cancer, cancer?

A

Its ability to metastasize

151
Q

How does cancer metastasize? Where does it usually metastasize to?

A

1) Lymphatic spread to regional and more distant lymph nodes
2) Hematogenous migration to far-away organs
3) Hematogenously to the liver, lung, brain, and bone

152
Q

How do epithelial tumors and adenocarcinomas typically spread?

A

Both through lymphatics and hematogenously

153
Q

Where do breast malignancies generally metastasize to?

A

Brain and bone

154
Q

Where do abdominal adenocarcinomas generally metastasize to?

A

Liver

155
Q

How do sarcomas metastasize and where do they generally metastasize to?

A

1) Sarcomas typically ignore the lymph nodes and go only blood-borne
2) Lungs

156
Q

What is the most common cause of death from cancer?

A

Primary tumors can kill if they are strategically located where they interfere with a vital function, but more cancer deaths come from metastatic spread, or systemic disease

157
Q

What is a requirement for local therapy to be able to cure cancer? What are the two therapies?

A

1) Local therapy can cure cancers only if they have not yet metastasized
2) Surgery and radiation

158
Q

Once cancer has metastasized, what are treatments focused on? What is the treatment is a cancer has metastasized?

A

1) Once cancer cells have migrated, treatments are only palliate, not curative. We cannot surgically resect and throw away the entire body; neither can we radiate someone from head to toe
2) We need systemic therapy for systemic disease: chemotherapy and (for some tumors) hormonal manipulations

159
Q

What negative effects do chemotherapy drugs have on the body and how do they have these effects?

A

Chemotherapy drugs target rapidly dividing cells and thus share some common side effects: They damage bone marrow, the lining of the GI tract, and hair follicles

160
Q

What is a specific negative effect of: 1) Adriamycin, 2) Bleomycin, 3) Cyclophosphamide, and 4) Platinum-based agents?

A

1) Myocardial damage
2) Pulmonary fibrosis
3) Hemorrhagic cystitis
4) Neurotoxicity

161
Q

What tumors occur almost exclusively in children?

A

Primary malignant tumors of bone occur almost exclusively in children

162
Q

What must be ruled out in all breast disease? How can this be done?

A

1) In all breast disease, cancer must be ruled out even if the presentation suggests benign disease
2) The only sure way to rule out cancer is to get tissue for the pathologist

163
Q

What demographic factor correlates best with the odds for breast cancer?

A

1) Age correlates best with the odds for breast cancer: virtually unknown in the teens, rare in young women, quite possible by middle age, and very likely in the elderly
2) The much-quoted statement “One of every 8 women in the US will develop breast cancer” is true only for those who have reached the age of 85

164
Q

Is breast cancer usually more benign or aggressive when it arises in young women?

A

Aggressive

165
Q

Mammography is an adjunct to what test that a physician can perform? How does it help?

A

1) Mammography is not a substitute for tissue diagnosis, but an adjunct to physical examination
2) Breast masses that may be missed by palpation may be seen in x-rays, and vice versa

166
Q

When should mammography screening begin?

A

As a regular screening exam, mammography should be started at age 40 (earlier if there is family history)

167
Q

When is mammography not done?

A

Mammograms are not done before age 20 (breast is too dense) or during lactation (all you see is milk), but they can be done if needed during pregnancy

168
Q

What is the most convenient, effective, and inexpensive way to biopsy breast masses?

A

Mammographically or sonographically guided multiple core biopsies have become the most convenient, effective, and inexpensive way to biopsy breast masses, whether they are palpable or are discovered by screening mammogram

169
Q

How old are patients usually who present with fibroadenomas? How do fibroadenomas present?

A

Fibroadenomas are seen in young women (late teens, early twenties) as a firm, rubbery mass that moves easily with palpation

170
Q

How is diagnosis of fibroadenoma established? Should a fibroadenoma be removed?

A

1) Either fine-needle aspiration (FNA) or sonogram is sufficient to establish diagnosis
2) Removal is optional (most women want them out, and we are happy to oblige)

171
Q

How old are patients usually who present with cystosarcoma phyllodes? What do these masses do over time? Can they become malignant?

A

1) Cystosarcoma phyllodes is seen in the late 20s
2) They grow over many years, becoming very large, replacing and distorting the entire breast, yet not invading or becoming fixed
3) Most are benign, but they have potential to become outright malignant sarcomas

172
Q

How are cystosarcoma phyllodes diagnosed? Do they need to be removed?

A

1) Core or incisional biopsy is needed (FNA is not sufficient)
2) Removal is mandatory

173
Q

How old are patients usually who present with mammary dysplasia (fibrocystic disease, cystic mastitis)? How does it present?

A

Mammary dysplasia (fibrocystic disease, cystic mastitis) is seen in the thirties and forties (goes away with menopause), with bilateral tenderness related to menstrual cycle (worse in the last 2 weeks) and multiple lumps that seem to come and go (they are cysts) also following the menstrual cycle

174
Q

When is only mammogram needed for diagnosis of mammary dysplasia and when are further steps required? What are the further steps, if needed?

A

1) If there is no “dominant” or persistent mass, mammogram is all that is needed, but if there is a persistent mass (presumably a cyst but potentially a tumor), further steps are required
2) Aspiration is done (not FNA, but aspiration with a bigger needle and syringe). If clear fluid is obtained and the mass goes away, that’s it. If the mass persists or recurs after aspiration, formal biopsy is required. If bloody fluid is aspirated, it should be sent for cytology

175
Q

How old are patients usually who present with intraductal papilloma? How does it present?

A

Intraductal papilloma is seen in young women (twenties to forties) with bloody nipple discharge

176
Q

What is needed to workup intraductal papilloma?

A

1) Mammogram is needed to identify other potential lesions, but it will not show the papilloma (they are tiny)
2) Galactogram may be diagnostic and guides surgical resection

177
Q

What is a galactogram?

A

Ductography (also called galactography or ductogalactography) is a special type of contrast enhanced mammography used for imaging the breast ducts. Ductography can aid in diagnosing the cause of an abnormal nipple discharge and is valuable in diagnosing intraductal papillomas and other conditions

178
Q

Which women develop a breast abscess? What is needed for treatment?

A

1) Breast abscess is only seen in lactating women (what appears to be a breast abscess at other times is cancer until proven otherwise)
2) Incision and drainage is needed, but biopsy of the abscess wall should be part of the procedure

179
Q

What should be suspected in any woman with a palpable breast mass? How does the index of this suspicion change with age?

A

Breast cancer should be suspected in any woman with a palpable breast mass, and the index of suspicion goes up with the patient’s age

180
Q

Aside from patient’s age, what are other strong indicators of breast cancer? Does a history of trauma rule out cancer?

A

1) Ill-defined fixed mass
2) Retraction of overlying skin
3) “Orange peel” skin
4) Recent retraction of the nipple
5) Eczematoid lesions of the areola
6) Reddish orange peel skin over the mass (inflammatory cancer)
7) Palpable axillary nodes
8) No

181
Q

How is breast cancer diagnosed during pregnancy? Is termination of pregnancy necessary to treat breast cancer?

A

1) Breast cancer during pregnancy is diagnosed exactly as if pregnancy did not exist and is treated the same way except for: no radiotherapy or hormonal manipulations at any time during the pregnancy, and no chemotherapy during the first trimester
2) No, it is not necessary

182
Q

What is the radiological appearance of breast cancer?

A

The radiological appearance of breast cancer is an irregular, spiculated mass with asymmetric density, architectural distortion, or fine microcalcifications that were not there in the previous mammogram

183
Q

What is the treatment of resectable breast cancer? What is the workup of lymph nodes in the presence of breast cancer?

A

Treatment of resectable breast cancer starts with either of two operations:

1) Small lesions, located far away from the nipple and areola of a large breast, are removed within only a segment of the mammary gland. The operation is called a lumpectomy, or segmental resection, and it must be followed by radiotherapy
2) Large tumors lying right under the nipple and areola, and occupying most of a small breast, require a simple total mastectomy and do not need subsequent radiation
3) If lymph nodes are not palpable in the axilla, either operation must include a sentinel node biopsy. If enlarged lymph nodes are palpable in the axilla, they are resected

184
Q

What is the standard form of breast cancer? What is the only variant with much worse prognosis? What are other variants and what is their prognosis and treatment method?

A

1) Infiltrating ductal carcinoma is the standard form of breast cancer
2) Inflammatory cancer is the only variant with much worse prognosis (and the need for pre-op chemotherapy)
3) Other variants (lobular, medullary, mucinous) have slightly better prognosis and are treated the same way as the standard infiltrating ductal. Lobular has higher incidence of bilaterality, but not high enough to justify bilateral mastectomy

185
Q

Can ductal carcinoma in situ (DCIS) metastasize? Does it have a high incidence of recurrence? What is the treatment if is confined to one quarter of the breast?

A

1) Ductal carcinoma in situ cannot metastasize (thus no axillary sampling is needed) but has very high incidence of recurrence if only local excision is done
2) Lumpectomy followed by radiation is used is the lesion (or lesions) is confined to one quarter of the breast

186
Q

When is total simple mastectomy recommended for DCIS? What do many practitioners follow this up with and why?

A

Total simple mastectomy is recommended for multicentric lesions throughout the breast; because of the possibility of missing an invasive focus in multicentric disease, many practitioners add a sentinal node biopsy in those

187
Q

How is inoperable cancer of the breast treated? What is inoperability based on?

A

1) Inoperable cancer of the breast is treated with chemotherapy (may also add radiation), and sometimes it is rendered operable
2) Inoperability is based on local extent (not metastases)

188
Q

When should adjuvant systemic therapy follow surgery in breast cancer treatment? When is chemotherapy used and when is hormonal therapy added?

A

1) Adjuvant systemic therapy should follow surgery in virtually all patients, particularly if axillary nodes are positive
2) Chemotherapy is used in most cases, and hormonal therapy is added if the tumor is receptor positive

189
Q

What type of breast cancer hormonal therapy do premenopausal women receive if given? Postmenopausal women? In what patients is hormonal therapy given alone for breast cancer?

A

1) Premenopausal women receive tamoxifen
2) Postmenopausal women receive anastrozole
3) Frail, old women with tumors that are not too aggressive may be offered hormonal therapy alone

190
Q

What finding suggests metastasis in women who recently had breast cancer?

A

Persistent headache or back pain (with areas of localized tenderness) in women who recently had breast cancer suggests metastasis

191
Q

What is a diagnostic test for breast cancer metastasis? How can brain metastases be treated? What is the favorite location in the spine for breast cancer to metastasize to?

A

1) MRIs are diagnostic
2) Brain metastases can be radiated or resected
3) The vertebral pedicles are the favorite location in the spine

192
Q

For breast cancer, what are infiltrated axillary nodes a marker of? What does removing these lymph nodes help with?

A

1) Cancer infiltrated axillary nodes tell us that systemic therapy is needed
2) If we choose to clean out an axilla that is full of cancer, we are only debulking. We are making the job of chemo and hormonal therapy a little easier by reducing the number of cells they have to kill

193
Q

Are most thyroid nodules benign or malignant? At what age do they occur? Does thyroid cancer affect thyroid function?

A

1) Most thyroid nodules are benign, but the few that are malignant must be diagnosed and treated
2) These can occur at any age
3) As a rule, thyroid cancer does not affect thyroid function

194
Q

How is the diagnosis made for thyroid cancer? What if the node is benign? What are the different types of thyroid cancer that can be diagnosed by FNA?

A

The diagnosis is typically made by fine needle aspiration (FNA), which is most cases indicates whetehr the node is benign (if so, follow up) or has papillary, medullary, or anaplastic cancer

195
Q

Which type of thyroid cancer cannot be easily diagnosed by FNA and what may be needed to be done next?

A

Follicular cancer is not easily diagnosed by FNA, and a lobectomy may be needed to determine if a follicular neoplasm is benign (adenoma) or malignant

196
Q

Is papillary thyroid cancer slow or fast growing? What dictates the extent of surgical resection?

A

1) Papillary cancer is very slow growing

2) The extent of surgical resection is dictated by the size of the tumor or the presence of metastatic nodes

197
Q

What is an advantage of doing a total thyroidectomy in the presence of follicular cancer?

A

1) Follicular cancer has rudimentary function: It can take radioactive iodine if it does not have to compete with normal thyroid tissue
2) Thus, a total thyroidectomy is always done for follicular cancer, because doing so permits use of radioactive iodine in the future to identify and treat any potential metastasis

198
Q

What cell type does medullary cancer of the thyroid develop from? How is it treated and why? Workup for what other condition is indicated in the presence of medullary thyroid cancer?

A

1) Medullary cancer comes from the C cells that make calcitonin (useful for follow-up)
2) It is aggressive, and radical surgery is justified
3) Workup for pheochromocytoma is indicated, as they often coexist (MEN, type 2)

199
Q

Anaplastic cancer of the thyroid is seen in young or old people? How quickly does it grow and what can be done?

A

1) Anaplastic cancer is seen in old people

2) It grows like wildfire, and often all that can be done for the patient is a tracheostomy

200
Q

What is hyperthyroidism treated with in most cases?

A

Hyperthyroidism is treated with radioactive iodine in most cases. There is a very limited role for surgery on patients who have a “hot adenoma”

201
Q

How is hyperparathyroidism most commonly found? What should be done next?

A

1) Hyperparathyroidism is most commonly found by serendipitous discovery of high serum calcium in blood tests (rarely seen in the full florid “disease of stones, bones, and abdominal groans”)
2) Repeat calcium determinations, look for low phosphorus, and rule out cancer with bone metastases. If findings persist, do parathyroid hormone (PTH) determination (and interpret in light of serum calcium levels)

202
Q

How frequently do asymptomatic patients with hyperparathyroidism become symptomatic? What is therefore justified to do?

A

1) Asymptomatic patients become symptomatic at a rate of 20% per year
2) Thus elective intervention is justified

203
Q

What percent of patients with hyperparathyroidism have single adenoma? Is removal curative? What test can be done to help locate the adenoma before surgery?

A

1) 90%

2) Removal is curative (sestamibi scan may help locate the culprit gland before surgery)

204
Q

How can Cushing syndrome be identified? What conditions are present?

A

1) Cushing can be identified at a glance by looking at the picture of a lovely young woman next to a picture of a “monster” who is the same lady a couple of years later. The “monster” has a round, ruddy, hairy face, buffalo hump, supraclavicular fat pads, obese trunk with abdominal stria, and thin weak extremities
2) Osteoporosis, diabetes, hypertension, and mental instability are also present

205
Q

What does workup of Cushing syndrome begin with? What does a negative test indicate?

A

1) Workup starts with an overnight low-dose dexamethasone suppression test
2) Suppression at low dosage rules out the disease (she is just a fat hairy lady)

206
Q

If dexamethasone suppression test is positive (no suppression), what is the next step in diagnosing Cushing syndrome? What if this test is elevated?

A

1) 24-hour urine-free cortisol is measured

2) If elevated, we go to a high-dose suppression test

207
Q

What does suppression at a higher dose dexamethasone indicate for Cushing syndrome? No suppression? Once the causal site is identified, what are the final steps?

A

1) Suppression at a higher dose identifies pituitary microadenoma
2) No suppression at either dosage identifies adrenal adenoma (or paraneoplastic syndrome)
3) Do appropriate imaging studies (MRI for pituitary, CT scan for adrenal) and remove the offending adenoma

208
Q

What diagnostic algorithm does the Mayo Clinic advocate that differs from the high-dose suppression test + imaging studies?

A

24-hour urinary collection for free cortisol levels (patients with this disease have levels 3 to 4 times the normal) is followed by measurement of corticotropin to differentiate pituitary adenomas from adrenal adenomas

209
Q

What is Zollinger-Ellison syndrome?

A

Zollinger-Ellison (gastrinoma) shows up as virulent peptic ulcer disease, resistant to all usual therapy (including eradication of Helicobacter pylori) and more extensive than it should be (several ulcers rather than one, ulcers extending beyond first portion of the duodenum)

210
Q

What symptom do some patients with Zollinger-Ellison syndrome present with? How should you workup and treat suspected Zollinger-Ellison syndrome?

A

1) Some patients have watery diarrhea
2) Measure gastrin and do secretin test if values are equivocal
3) Locate the tumor with CT scan (with contrast) of the pancreas and nearby areas
4) Remove it
5) Omeprazole helps those with metastatic disease

211
Q

Why and when does an insulinoma produce CNS symptoms?

A

Insulinoma produces CNS symptoms because of low blood sugar, always when the patient is fasting

212
Q

What is the differential diagnosis of insulinoma with?

A

Differential diagnosis is with reactive hypoglycemia (attacks occur after eating) and with self-administration of insulin

213
Q

How can you determine if someone has hypoglycemia induced by self-administration of insulin?

A

Patients have reason to be familiar with insulin (some connection with the medical profession, or with a diabetic patient), and in plasma assays they have high insulin but low C-peptide. In insulinoma, both are high

214
Q

What imaging should be done to identify an insulinoma? What should be done once the tumor is located?

A

1) CT (with contrast) of pancreas is done to locate tumor

2) Remove it

215
Q

In a patient with suspected insulinoma, levels of what drug aside from insulin needs to be measured in the workup?

A

Some medically sophisticated patients are using sulfonylureas to induce endogenous insulin secretion, and defeat the diagnostic value of C-peptide. Levels of those drugs need to be measured in the workup

216
Q

What is nesidioblastosis?

A

Nesidioblastosis is a devastating hypersecretion of insulin in the newborn, requiring 95% pancreatectomy

217
Q

How does a glucagonoma present?

A

Glucagonoma produces severe migratory necrolytic dermatitis, resistant to all forms of therapy, in a patient with mild diabetes, a touch of anemia, glossitis, and stomatitis

218
Q

What is a diagnostic test for glucagonoma? What test is used to locate the tumor? Is resection curative?

A

1) Glucagon assay is diagnostic
2) CT scan is used to locate tumor
3) Resection is curative

219
Q

What can help in patients with metastatic, inoperable glucagonoma?

A

Somatostatin and streptozocin can help those with metastatic, inoperable disease

220
Q

What can primary hyperaldosteronism be caused by? What is the key finding in both cases? What are some other findings?

A

1) Primary hyperaldosteronism can be caused by an adenoma or by hyperplasia
2) In both cases the key finding is hypokalemia in a hypertensive (usually female) patient who is not on diuretics
3) Other findings include modest hypernatremia and metabolic alkalosis

221
Q

Are levels of aldosterone high or low in primary hyperaldosteronism? Renin?

A

Aldosterone levels are high, whereas renin levels are low

222
Q

How can response to postural changes help in the diagnosis of etiology of primary hyperaldosteronism?

A

Appropriate response to postural changes (more aldosterone when upright than when lying down) suggests hyperplasia (which is treated medically), whereas lack of response (or inappropriate response) is diagnostic of adenoma

223
Q

How is adrenal adenoma identified? Can surgical removal provide cure?

A

1) Adrenal CT scans localize it

2) Yes

224
Q

In which patients is pheochromocytoma typically seen in? Why can diagnosis be frustrating?

A

1) Pheochromocytoma is typically seen in thin, hyperactive women who have attacks of pounding headache, perspiration, palpitations, and pallor (at which time they have extremely high blood pressure)
2) By the time patients are seen, the attack has subsided and the pressure may be normal, leading to a very frustrating lack of diagnosis. Patients who have sustained hypertension are easier to diagnose

225
Q

How should workup of pheochromocytoma begin? What should be done next? Are tumors usually small or large? What is required prior to surgery?

A

1) Start workup with 24-hour urinary determination of vanillylmandelic acid (VMA-easy to do, but may give false positives), metanephrines (more specific), or free urinary catecholamines
2) Follow with CT scan of adrenal glands or radionuclide studies if looking for extraadrenal sites
3) Tumors are usually large
4) Surgery requires careful pharmacologic preparation with alpha-blockers

226
Q

How do patients with coarctation of the aorta typically present? What does CXR show? What is the diagnostic test? Is surgical correction curative?

A

1) Coarctation of the aorta may be recognized at any age, but patients typically are young and have hypertension in the arms, with normal pressure (or low pressure, or no clinical pulses) in the lower extremities
2) Chest x-ray shows scalloping of the ribs (erosion from large collateral intercostals)
3) Spiral CT scan enhanced with intravenous dye (CT angio) is usually diagnostic
4) Yes, surgical correction is curative

227
Q

In which two groups do you usually see renovascular hypertension? What do you see in both groups that suggests the diagnosis?

A

1) Young women with fibromuscular dysplasia
2) Old men with arteriosclerotic occlusive disease
3) In both groups hypertension is resistant to the usual medications, and a telltale faint bruit over the flank or upper abdomen suggests the diagnosis

228
Q

What is the workup of renovascular hypertension? What is therapy and when is it used?

A

1) Workup is multifactorial, but duplex scanning of the renal vessels and CT angio have prominent roles
2) Therapy is imperative in the young women, usually balloon dilatation and stenting; but it is much more controversial in the old men who may have short life expectancy from the other manifestations of the arteriosclerosis