GI- small bowel, colorectal and anus Flashcards
Anatomy and physiology
1) where does nutrient absorption occur
2) where does water absorption occur
3) Duodenum
a-Most common location for ulcers
b- contains ampulla of Vater (duct of wirsung) and duct of santorini
c- which portions are retroperitoneal
d- where is there a transition point in the duodenum
e- where is vascular supply (arteries and where they run)
1) small bowel
2) small and large bowel
3) a- duodenal bulb (1st portion)
b- 2nd portion (Descending)
c- Descending (2nd) and transverse (3rd) portions are retroperitoneal
d- bw 3rd and 4th portions at the acute angle between the aorta (posterior) and SMA (anterior)-> can get SMA compression of duodenum here if angle too acute
4) superior (off gastroduodenal artery) and inferior (off SMA) pancreaticoduodenal arteries. Both have anterior and posterior branches and many commincations
Small bowel Anatomy and physiology 1) what is maximum site of all absorption except for B12, bile acids, iron and folate 2) where is B12, bile acids (conjugated and non-conjucated), iron and folate absorbed 3) Jejunum a- length b- vascular supply c- % of water and NaCl absorbed here 4) Ileum a- length b-vascular supply
1) jejunum
2) B12 (terminal ileum), bile: non-conjugated in ileum and conjugated in terminal ileum, iron (duodenum) and folate (Terminal ileum)
3) a-100cm, long vasarecta, circular muscle folds
b- SMA
c-95% NaCl and 90% of water
4) 150 cm, short vasa recta, flat
b- SMA
Small bowel Anatomy and physiology
1) enzymes contained in intestinal brush border
2) normal size (circumference) of small bowel/transverese colon/cecum
3) branch of SMA that supplies ileum/cecum
1) maltase, sucrase, limit dextrinase, lactase
2) small bowel- 3cm/ transverse colon-6cm/ cecum 9cm
3) ileocolic
Small bowel cell types, which cells:
1) secrete mucin
2) have secretory granules and enzymes
3) do amine precursor uptake and decarboxylation (APUD), 5-hydosytryptamine release and are the precursor for carcinoid
4) have alkaline solution
5) are lymphoid tissue, and where are they increased in number
6) are Ag-presenting cells in intestinal wall
1) goblet cells
2) Paneth cells
3) Enterochromaffin cells
4) Brunner’s glands
5) Peyer’s patches, increased in ileum
6) M cells
Small bowel Anatomy and physiology
1) where is IgA released
2) what part of intestines has both heme and Fe transporters
3) phases of the migrating motor complex (gut motility)
4) most important hormone in migrating motor complex and what phase does it act on
1) released into gut and in mother’s milk
2) small bowel
3) Phase I- rest; Phase II- acceleration and gallbladder contraction; phase III- peristalsis; Phase IV- deceleration
4) motilin, acts on phase III= peristalsis
Bile salts (Acids)
1) what % are reabsorbed
2) what % is active vs passive resorption and what type of bile salts are absorbed with each and where do they occur
3) why do gallstones form after terminal ileum resection
1) 95%
2) 50/50
active- conjugated bile salts in terminal ileum via Na/K-ATPase only
passive- non-conjugated bile salts- 45% in ileum and 5% in colon
3) malabsorption of bile salts
Short Gut Syndrome
1) how is dx made
2) sx
3) what nutritional deficits do these patients have
4) What does the Sudan Red stain check for
5) what does the Schilling test check for
6) how much bowel do you need to survive off TPN
7) rx
1) on symptoms, not gut length
2) diarrhea, steatorrhea (sudan red stain), weight loss, nutritional deficiency
3) lose fat, B12, electrolytes, water
4) looks for fecal fat
5) checks for B12 absorption (radiolabled B12 in urine)
6) 75cm or 50cm with competent ileocecal valve
7) restrict fat, PPI to reduce acid, Lomotil (diphenoxylate and atropine)
Causes of steatorrhea
1) mechanism if gastric hypersecretion of acid is the cause
2) mechanism if interruption of bile salt resorption (ie- TI resection) is the cause
3) rx
1) decreased pH-> inc intestinal motility-> interferes with fat absorption
2) interferes with micelle formation and fat absorption
3) control diarrhea (Lomotil), dec oral intake, especially fats, pancrease and PPI
Non healing EC fistula
1) causes that interfere with healing
2) what type of fistulas are more likely with proximal bowel (high-or low output) and less likely to close with conservative management
3) what location of fistulas are more likely to close
4) in pt with ECF and persistent fever what should you check for
5) rx
1) FRIENDS: foreign body, radiation, IBD, epithelialization, Neoplasm, Distal obstruction, Sepsis/infection
2) high-output are more likely proximal and less likely to heal
3) colonic fistulas
4) r/o abscess- fistulogram, CT abd, upper GI with small bowel followthrough
5) NPO, TNP, skin protection (stoma appliance), octreotide. If need surgery-> resect segment containing fistula and perform primary anastomosis
Bowel Obstruction and most common causes:
1) without previous surgery
a- small bowel
b- large bowel
2) with previous surgery
a- small bowel
b- large bowel
3) why is aggressive fluid resuscitation important in SBP
4) cause of air with bowel obstruction
5) what % are cured with conservative management
6) indications for surgery
1) a- hernia; b-cancer
2) a-adhesions, b-cancer
3) 3rd spacing of fluid into bowel lumen occurs
4) swallowed nitrogen
5) 80% of pSBO and 40% of complete SBO
6) progressing pain, peritoneal signs, fever, increasing WBCs (all signs of strangulation or perforation), or failure to resolve
Gallstone Ileus
1) cause
2) Radiologic findings
3) rx
1) fistula bw gallbladder and 2nd portion of duodenum-> SBO from stone in terminal ileum
2) air in biliary tree in pt with SBO
3) remove stone from TI. can leave GB and fistula if pt too sick. if not too sick-> cholecystectomy and close duodenum
Meckles diverticulum
1) rule of 2’s
2) embryologic cause
3) MC presentation in kids and adults
4) MC tissue found in meckel’s
5) type of tissue most likely to be symptomatic in meckels and symptoms
6) rx of incidental meckel’s
7) rx of meckels with uncomplicated diverticulitis or bleeding
8) Dx
1) located 2ft from ileocecal valve; 2% of population have it; usually presents in the 1st 2 years of life with bleeding; a true diverticulum
2) failure of closure of the omphalomesenteric duct
3) accounts for 50% of all painless lower GI bleeds in children bleeding
6) don’t remove unless gastric mucosa suspected (feels thick or has very narrow neck)
7) diverticulectomy if uncomplicated. need segmental rsxn if complicated (ie-perf), neck >1/3 of diameter of normal bowel lumen or diverticulitis involves the base
8) Meckel’s scan (99Tc) if trouble localizing (mucosa lights up)
Duodenal diverticula
1) what disease process must be r/o
2) rx
3) frequency of diverticula in the 3 diff segments of small bowel
1) r/o gallbladder-duodenal fistula
2) observe unless perf’d, bleeding or causing obstruction or highly symptomatic then do segmental resection. if juxta-ampullary usually need choledochojejunostomy for biliary or ERCP with stent for pancreatitis symptoms (avoid whipple)
3) duodenum> jejunum>ileum
Crohn’s Disease
1) age at 1st presentation, ethnicity with increased frequency
2) extraintestinal manifestations
3) what part of GI tract is usually spared
4) MC area involved
5) what % first present with anal/perianal dz and MC sx and rx
6) MC sites for initial presentation
1) 15-35 yo, inc in ashkenazi Jews
2) arthritis, arthralgias, pyoderma gangrenosum, erythema nodosum, ocular diseases, growth failure, megaloblastic enemia from folate and vit B12 malabsorption
3) rectum
4) Terminal ileum
5) 5%, rx- flagyl. large skin tag MC for anal dz.
6) TI and cecum (40%)> Colon only (35%)> small bowel only (20%) >perianal (5%)
Crohn’s Disease
1) dx
2) Medical Rx
3) what % eventually need an operation
1) colonoscopy with path showing transmural involvement, segmental dz (skip lesions), cobblestoning, narrow deep ulcers, creeping fat, fistulas and granulomas
2) 5-ASA and loperamide for maintenance. Steroids for acute flares.
Remicaide (infliximab; TNF-alpha inhibitor)- for fistulas or steroid resistant disease. NO agents affect the natural course of disease. TPN may induce remission and fistula closure with small bowel dz
3) 90%
Crohn’s Disease
1) Surgical indications
2) rx of pts with diffuse disease of colon
3) Can you do pouches or ilio-anal anastomosis with Crohn’s disease
4) rx of incidental finding of IBD in pt with presumed appendicitis and nl appendix.
1) obstruction that doesn’t resolve with conservative management, abscess (perc drain), Megacolon, hemorrhage (unusual), blind-loop obstruction, Fissures (no lateral internal sphincteroplasty), perineal fistula- unroof and r/o abscess, anorectovaginal fistula- may need rectal advancement flap, pos colostomy. Just get 2cm away from gross dz, no need for clear margins
2) proctocolectomy and ileostomy
3) no
4) remove appendix to avoid future confusion
Crohn’s disease
1) when to consider sticturoplasty
2) recurrence rate requiring surgery for Crohn’s disease after resection
3) Complications from removal of Terminal Ileum
4) Colon CA risk of Crohn’s pancolitis compared to risk from UC
1) if pt has mult bowel strictures and need to save length. Not good for 1st surgery. Has 10% leak/abscess/fistula rate.
2) 50%
3) megaloblastic anemia (dec B12 uptake)
osmotic diarrhea and steatorrhea from dec bile salt uptake
Ca oxalate kidney stones 2/2 dec oxalate binding to Ca bc of intraluminal fat binding Ca instead-> inc oxalate absorbed-> released in urine-> hyperoxaluria
Gallstones from malabsorption of bile salts
4) same risk
Carcinoid Tumors 1) hormones released by what cells and how to measure 2) MC site 3) pts with tumors where are at inc risk for multiple primaries and second unrelated malignancies 4) Carcinoid rx if: a- in appendix b- anywhere else in GI tract c- unresectable 5) Causes of false 5-HIAA
1) serotonin (produced by Kulchitsky cells (enterochromaffin cells)). Breakdown product is 5-HIAA which can be measured in the urine. Bradykinin also released
2) appendix (50%), then ileum and rectum
3) small bowel tumors
4) a- if appendectomy; if >2cm or involving base=>right hemicolectomy
b-treat like CA (segmental rsxn with lymphadenectomy)
c- chemo: streptozocin and 5FU, usually just for resectable disease
5) fruits
Carcinoid syndrome
1) where is the tumor if having this syndorme?
2) sx and the responsible hormones
3) best test for localizing tumor not seen on CT
4) serum test that is highest sensitivity for detecting carcinoid tumor
5) treatment
1) bulky liver mets
2) Kallikrein-> flushing; serotonin-> diarrhea; bradykinin-> asthma-type symptoms
3) Octreotide scan
4) Chromogranin A level
5) if resect liver mets, also resect GB in case of future embolization
octreotide-> for carcinoid syndrome palliation.
Aprotinin for bronchospasm
Phenothiazine (alpha-blockers) for flushing
Intussusception in adults
1) causes
2) MC presentation
3) rx
1) small bowel or cecal tumors (worrisome in adults bc often malignant lead point)
2) obstruction
3) resection
Benign Small Bowel tumors 1) Adenomas a- MC location; b- sx; c- rx 2) Puetz-Jeghers Syndrome a- inheritance pattern b- associated benign tumors c- associated malignancies
1) a- duodenum; b- bleeding/obstruction; c-rsxn often with endoscopy
2) a- autosomal dominant
b- small and large bowel hamartomasl pts also have mucocutaneous melanotic skin pegmentation
c- extraintestinal malignancies (MC- breast CA) and small risk of GI malignancies but don’t do prophylactic colectomy.
Malignant small bowel tumors 1) MC malignant SB tumor 2) Duodenal CA risk factors 3) Adenocarcinoma a- how common b- MC location within SB c- sx d- rx
1) adenocarcinoma (but rare overall)
2) FAP, Gardner’s polyps, adenomas, von Recklinghausen’s
3) a- rare
b- duodenal
c- obstruction, jaundice
d- resection and adenectomy. Whipple if in 2nd portion of duodenum
Small bowel Leiomyosarcoma
1) MC location
2) how to differentiate with leiomyoma
3) how to differentiate from GIST
4) rx
1) jejunum and ileum; most extraluminal
2) hard. >5mitoses/hpf, atypia, necrosis
3) test for c-KIT (GIST if positive)
4) resection. No adenectomy required
Small bowel lymphoma
1) MC location
2) associated diseases
3) MC type of lymphoma
4) Dx
5) Rx if a- in 1st or 2nd portion of duodenum; b- if anywhere else
6) prognosis
1) ileum
2) Wegener’s SLE, AIDS, Crohn’s, celiac sprue
3) NHL B cell type
4) abdominal CT, node sampling
5) a- Chemo-XRT, NO whipple; b- wide en bloc resection including nodes
6) 40% 5-year survival rate