Rubin's path unit 6 Flashcards

1
Q

GI 7: Sliding hiatal hernias vs. paraesophageal hiatal hernia:

A

SHH: enlargement of hiatus and laxity of the circumferential CT allows cap of gastric mucosa to move upward above diaphragm;
PHH: herniation of a portion of the gastric fundus alongside the esophagus through a defect in the diaphragmatic CT membrane

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2
Q

GI 8: Chemical injury to the esophagus usually reflects

A

accidental poisoning in children, attempted suicide in adults, or contact with meds; ingestion of strong acids produces an immediate coag necrosis in the esophagus, resulting in a protective eschar that limits injury and further chem penetration;
strong alkaline solutions accompanied by LIQUEFACTIVE NECROSIS

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3
Q

GI 12: The most common type of esophagitis is

A

reflux esophagitis, often found in conjunction with a sliding hiatal hernia but could also arise through an incompetent lower esophageal sphincter without demonstrable anatomical lesion

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4
Q

GI 19: Melena refers to

A

black, tarry stools composed largely of blood from the upper digestive tract that has been processed by the action of gastric juices; think CHRONIC PEPTIC ULCER DISEASE

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5
Q

GI 21: ZE syndrome characterized by

A

unrelenting peptic ulceration in the stomach or duodenum (or even proximal jejunum) by action of tumor-derived gastrin

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6
Q

GI 24: Menetrier disease is an

A

uncommon disorder of the stomach characterized by enlarged rugae; often accompanied by severe loss of plasma proteins (including albumin) from altered gastric mucosa. Disease can occur in kids with CMV and in adults with overexpression of TGF-alpha

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7
Q

GI 25: GI stromal tumors are derived from

A

pacemaker cells of Cajal; include a vast majority of mesenchyme-derived stromal tumors of the entire GI tract. Gastric GISTs are usually submucosal and covered by intact mucosa. Look for spindle cells with vacuolated cytoplasms and low malignant potential

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8
Q

GI 27: Bezoars are

A

foreign bodies in the stomach that are composed of food or hair that have been altered by the digestive process; trichobezoar is a hairball (long-haired girl eating own hair like Rapunzel) and phytobezoars are concretions of plant material

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9
Q

GI 31: Hyperplastic polyps are

A

small, sessile mucosal excrescenes that display exaggerated crypt architecture. Think of them as the most common polypoid lesions of the colon and are particularly frequent in the rectum. Look for elongated crypts and cystic dilations

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10
Q

GI 32: Tubular adenomas are

A

smooth-surface lsions, usually less than 2 cm in diameter, and often have a STALK. Look for closely packed epi tubules, which may be uniform or irregular with excess branching. Dysplasia and carcinoma often develop in tubular adenomas.

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11
Q

GI 37: Metastatic carcinoma is

A

most common malignant disorder affecting the peritoneum

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12
Q

GI 44: Crohn disease is a

A

transmural chronic inflamm disease that may affect any part of the digestive tract; intestinal obstruction and fistulas are most common intestinal complications of Crohn disease

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13
Q

GI 50: What are some sequelae of ulcerative colitis?

A

Arthritis, uveitis and skin lesions like erythema nodosum and pyoderma gangrenosum;

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14
Q

GI 51: Nephrotic syndrome in kids along with systemic infection seeding ascitic fluid with bacteria can lead to

A

spontaneous bacterial peritonitis that doesn’t occur with obvious perforation

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15
Q

GI 52: Diverticulitis results from

A

irritation caused by retained fecal material that obstructs the lumen of a diverticulum

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16
Q

GI 58: Anorectal malformations are associated with

A

relation of the terminal bowel to the levator ani muscle

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17
Q

GI 59: How do anorectal malformations result? What else can develop?

A

Arrested development of the caudal region of the gut in the first 6 mos of fetal life;
fistulas b/w the malformation and the bladder, urethra, vagina, or skin

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18
Q

GI 61: Stercoral ulcers result from

A

pressure necrosis of the mucosa caused by the fecal mass impacted; complications include rectal bleeding and perforation

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19
Q

GI 62: Mucocele refers to a

A

dilated mucous-filled appendix; if nonneoplastic, you have retention of mucus in the appendiceal lumen;
in mucinous cystadenoma or mucinous cystadenocarcinoma, the dilated appendix is lined by a villous adenomatous mucosa

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20
Q

GI 63: Radiation therapy for malignant disease of the pelvis or abdo

A

may be complicated by injury to the SI and colon

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21
Q

LB 7: Acute viral hepatitis path changes include

A

disarray of liver cell plates, ballooning degen of hepatocytes, IC and EC bile statis, apoptotic (COUNCILMAN) bodies, and mononuclear inflamm cell infiltrates

22
Q

LB 12: Autoimmune hepatitis is a type of

A

chronic hepatitis, which is associated with circulating autoAbs (aninuclear Ab’s) and high levels of serum immunoglobulins; usually accompanied by other autoimmune diseases like Sjogren, SLE, etc
RESPONDS TO STEROIDS

23
Q

LB 13: Cholangiocarcinoma can originate

A

anywhere in the biliary tree, from the large intrahepatic ducts at the porta hepatis to the smallest bile ductules at the periphery of the hepatic lobules;
think liver fluke C. sinensis

24
Q

LB 14: In hepatorenal syndrome, this occurs

A

in setting of cirrhosis and heralds a poor prognosis; think renal hypoperfusion, including oliguria, azotemia, and increased levels of serum creatinine; microscopically the KIDNEY APPEARS NORMAL

25
Q

LB 17: Common cause of massive hepatic necrosis is

A

HBV; liver appears shrunken, capsule is wrinkled, and the parenchymal tissue is soft and flabby;
the massive hepatic necrosis can lead to fulminant hepatic failure

26
Q

LB 20: Acute alcoholic hepatitis characterized by

A

hepatic steatosis, hydropic swelling of hepatocytes, focal hepatocellular necrosis, neutrophilic infiltration, and cytoplasmic hyaline inclusions within the hepatocytes (Mallory bodies)

27
Q

LB 25: Budd-Chiari a

A

congestive disease of the liver caused by occlusion of the hepatic veins and their tributaries; think thrombosis of hepatic veins

28
Q

LB 27: Most complications associated with cholelithiasis

A

are related to obstruction of the biliary tree

29
Q

LB 29: What is the best way to assess extent of liver disease in a patient with viral hepatitis? What can you see with this method?

A

Liver biopsy; ballooning degen of liver cells, IC and EC bile stasis, acidophilic bodies, and mononuclear cell infiltrate seen

30
Q

LB 30: Chemicaly-induced hepatic injury is classified as “predictable” when; indirect injury of the liver is caused by

A

toxicity is immediate and dose-dependent;

metabolites and free rads that are produced as byproducts of xenobiotic metabolism

31
Q

LB 31: Patients with persistent HBV infection have a

A

200-fold increased risk of developing primary HCC

32
Q

LB 34: alpha1-antitrypsin deficiency characterized by

A

presence of round-to-oval cytoplasmic globular inclusions of misfolded alpha1-antitrypsin proteins in hepatocytes;
glboules stain red with PAS after removing glycogen with diastase

33
Q

LB 35: pyogenic liver abscesses are caused by

A

staph, strep, and gram-neg enterobacteria; these bacteria gain access to the liver by direct extension from contiguous organs or through the portal vein or hepatic artery; maybe diverticulitis and inflamm bowel diseases

34
Q

LB 36: Massive hepatic necrosis the most feared variant of

A

acute hepatitis; look for massive death of hepatocytes, leaving a collapsed collagenous framework

35
Q

LB 37: What can suggest acetaminophen toxicity?

A

Centrilobular necrosis

36
Q

LB 43: Andersen disease is

A

also known as glycogen storage disease type IV, an autosomal recessive genetic disease caused by deficiency of a glycogen-branching enzyme; without this enzyme, you have accumulation of abnormal glycogen (amylopectin) in liver, muscle, and other tissues

37
Q

LB 44: Acute intermittent porphyria is the

A

most common genetic porphyria; it’s AD and caused by deficiency of porphobilinogen deaminase activity in liver

38
Q

LB 45: Histologic features of neonatal hepatitis include

A

prolonged cholestasis, inflamm, and cell injury; look for giant cell transformation of hepatocytes

39
Q

P 9: Majority of pancreatic carcinomas arise from

A

pancreatic duct epi; acinar cell carcinoma much less common

40
Q

ID 13: P jireveci causes

A

progressive, often fatal pneumonia in persons with impaired cell-mediated immunity and on of the most common opportunistic pathogens in persons with AIDS;
trophozoites attach to alveolar lining, and they feed, enlarge, and transform into cysts within host cells

41
Q

ID 17: RSV is a(n) _____ virus, the major cause of

A

RNA; bronchiolitis and pneumonia in infants; think expiratory and inspiratory wheezing, cough, and hyperexpansion of both lung fields;
hyperinflation, interstitial infiltrates, segmented atelectasis

42
Q

ID 19: Measles virus is a(n) ____ virus that causes

A

RNA; acute, highly contagious, self-limited illness with UR tract symptoms, fever, and rash;
think respiratory droplets and secretions, and look for skin rash and Koplik spots on posterior buccal mucosa

43
Q

ID 21: Measles virus can cause fusion of

A

infected cells, producing multinucleated cells termed “Warthin-Finkeldey giant cells”;

44
Q

ID 24: Rhizopus, Mucor, Rhizomucor, and Absidia can produce

A

necrotizing opportunistic infections that begin in the nasal sinuses or lungs; Mucor ubiquitous in the nasal sinuses and invades surrounding tissues, and look for hard palate or nasal cavity covered by black crust

45
Q

ID 30: Toxoplasmosis is a

A

potentially necrotizing meningoencephalitis with infection of the CNS; can see ocular infections causing chorioretinitis

46
Q

ID 32: Rickettsia typhi characterized by

A

fever, severe headache, and myalgias, followed by appearance of maculopapular rash on the upper trunk and axillary folds, going to extremities

47
Q

ID 37: MAC is a

A

rare granulomatous pulm disease in immunocompetent persons, but is a progressive systemic disorder in patients with AIDS; can see progressive involvement of small bowel to produce malabsorption and diarrhea

48
Q

ID 51: Erysipelas is an

A

erythematous swelling of the skin caused chiefly by S pyogenes infection

49
Q

ID 54: Yellow fever is an

A

acute hemorrhagic fever, associated with hepatic necrosis and jaundice; caused by mosquito-borne flavivirus (tropism for liver cells), with Councilman bodies and microvesicular fatty changes

50
Q

ID 55: Visceral leishmaniasis presents with

A

persistent fever, progressive weight loss, HSM, anemia, thrombocytopenia, and leukopenia; can develop darkening of the skin

51
Q

ID 61: If humans ingest eggs from Taenia solium,

A

eggs release oncospheres and differentiate to cysticerci and they can lodge in tissues like the brain and get headaches and seizures