10. GI Pathoma Flashcards

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1
Q

Tracheo-Esophageal Fistula

most common type?

A

Connection between Trach and the esophagus

  • esophageal atresia w/ distal esophagus connecting to trach
  • can cause polyhydramnios (cant swallow anything)
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2
Q

Plummer-Vinson syndrome

A

Esophageal webbing

Iron deficiency anemia

Beefy red tongue (atrophic glossitis)

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3
Q

Zenker Diverticulum

where does it outpouch?

how does it present-

A

Outpouching of the pharyngeal mucosa through a defect in the wall

  • Killian Triangle
  • halitosis, dysphagia
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4
Q

Mallory-Weiss syndrome

whos the main to get this

A

Lacerations at the gastroesophageal junction due to Severe vomiting

painful hematemesis (bloody vomit)

-alcoholics and bullemics

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5
Q

Boerhaave syndrome

A

Transmural, distal esophageal rupture due to violent retching

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6
Q

Achalasia

what causes this

A

Absence of relaxation of the LES (lower esophageal sphincter)

-loss of Myenteric (Auerbach) plexus

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7
Q

GERD

what anatomy fuck up can cause this?

A

reflux of acid from the stomach due to Decr. LES tone

-sliding hiatal hernia

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8
Q

Gastroschisis

A

abdominal contents coming thru abdominal folds

(Not covered by peritoneum)

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9
Q

Omphalocele

A

Herniation of abdominal contents

Covered by peritoneum (silver cap)

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10
Q

Pyloric Stenosis

when does it happen/ what does the mass look like/ how is the vomit?

A

Hypertrophy of the pyloric smooth muscle

  • doesnt present at birth. usually in 2-6 weeks.
  • olive shaped mass

-non billious vomiting

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11
Q

Barrett esophagus

whats it caused by?

A

Metaplasia of

nonkeratinized stratified squamos cells ->

nonciliated columnar /goblet cells

  • chronic GERD
  • increased risk of esophageal adenocarcinoma
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12
Q

What are the two types of Esophageal cancers?

where are they/how do you get them?

A

Squamos Cell - upper 2/3. alc, hot liquids, strictures, smoking, achalasia (more common world wide

Adenocarcinoma - lower 1/3. chronic GERD, Barrett, obesity (common in America)

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13
Q

Acute gastritis

Main causes/ common among who?

A
  • Too much acid/ too little mucosa protection
  • alcoholics or NSAID users
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14
Q

Chronic Gastritis

A

Increase risk of gastric cnacer

-H. Pylori (MALToma)/ Autoimmune (antibodies to parietal cells and intr

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15
Q

What are parietal cells?

What receptors are on it?

where are they located?

A

Secretes acid in the stomach

Ach, Gastrin, Histamine receptors

-body and the fundus

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16
Q

where is gastrin produced?

A

G cells (in the antrum and duodenum)

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17
Q

Peptic Ulcer Dz

Duodenal ulcer

what other things can cause it?

where is perforation most common?

what can happen with posterior ulcers

A
  • Pain Decreases with meals (when you eat, the duodenum secretes protective coat (Brunners glands) cuz it knows food/acid is bout to come in)
  • decr. mucsoal protection/incr. gastric acid (h. pylori)
  • -Zollinger-Ellison syndrome* (Gastrinoma)
  • anterior wall of stomach
  • rupture of Gastroduodenal artery/ acute pancreatits
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18
Q

Peptic Ulcer Dz

Gastric Ulcers

whats a main cause?

where is the rupture? what would bleed.

A

pain becomes Greater with meals (stomach knows food is coming down so it secretes more acid)

-NSAIDS

-lesser curvature of stomach (bleeding from Left gastric artery)

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19
Q

Gastric Cancer (Adenocarcinoma)

Intestinal Vs Diffues type

what do they look like/where are they found/risk factors

-how does gastric carcinoma present (the rare signs)

A

malignant proliferation of surface epithelial cells in the stomach

Intestinal: irregular ulcer with f’d up margins. lesser curvature. rf: H.pylori, nitrosamines (smoked food), gastritis, Blood type A

Diffuse: Signet ring cells (mucin filled cells with periph nuclei) that infiltrate gastric wall. Stomach wall grossly thickens

-Acanthosis Nigrans (skin thickening in axilla) / Leser-Trelat (morgan freemans all over their skin- sub keratosis)

20
Q

What are the three mets of stomach cancer?

A

Virchow node: left supraclavicular node

Kruckenberg tumor: bilateral met to ovaries (mucin & signet ring cells)

Sister mary Joseph: Subcutaneous periumbilical met

21
Q

What is duodenal atresia associated with?

what are some clinical features

A

Downsyndrome

-polyhydramnios, distension of the stomach “Double bubble” on xray, billious vomiting

22
Q

Meckel Diverticulum

what causes it?

A

True diverticulum - outpouching of ALL THREE layers off of the intestine near the ileocecal valve

-failure of Vitelline duct

23
Q

Volvulus

where do they happen in elderly/young

A

Twisting of bowel around its mesentary

results in obstruction of bowel and infarction of arteries

elderly: Sigmoid colon

Young: Cecum

24
Q

intussusception

most common location?

clinical finding?

A

telescoping of the bowel

  • ileocecal junction
  • currant jelly stool
25
Q

Acute mesenteric ischemia/infarction

whats the most often occlusion

clinical presentaiton

A

Blockage of intestinal blood flow

  • SMA (superior mesenteric Arterty)
  • Pain out of Proportion*
26
Q

Lactose Intolerance

A

decreased function of the lactase enzyme along the brushboarder

27
Q

Celiac Dz

what does having this cause?

what skin condition does it cause?

lab findings?

biopsy?

where in the gi is affected

A

Autoimmune damage to small bowel villi due to Gluten/Gliadin (protein found in wheat)

  • malabsorption and steatorrhea.
  • dermatitis herpetiformis (deposition of IgA in papilla)

IgA antibodies to endomysium, tTg, gliadin

Flattening Villi / Crypt hyperplasia

-Duodenum

28
Q

Tropical Sprue

A

similar to celiac dz /tropics

responds to antibiotics

29
Q

Whipple Dz

what section of Gi is involved

what does this lead to?

A

infection w Tropheryma whipplei

foamy macrophages (they eat the t. whipp)

CAN

Cardio probs, Arthralgas, Neuro probs

Lamina propria

-fat malabsorption/ steatorrhea

30
Q

Carcinoid tumor

most common site?

what does it usually secrete?

symptoms once met to liver?

A

malignant prolif of neuroendocrine cells

positive for chromogranin

-small bowel

-Serotonin

bronchospasm, diarrhea, flushing of the skin

31
Q

Irritable Bowel Syndrome

who mainly gets it?

A

Reccurent/Rlapsing abdominal pain

32
Q

Inflammatory Bowel Dz

Ulcerative collitis

location? diarrhea?

key hallmarks?

complication? p-anca?

what protects against UC?

A

Mucosal and submucosal inflam only

-Colon (duh) **Starts at rectum and works it way up

(continuous) Bloody poop

  • Crypt abscesses (filled with neutrophils) / LEAD PIPE / Psuedopolyps
  • Toxic megacolon or Rupture
  • Positive P-ANCA
  • Smoking
33
Q

Inflammatory Bowel Dz

Chrons DZ

location? type of poop?

hallmarks?

whats it look like on imaging

A

Full thickness(Transmural) of inflam.

anywhere from mout to the anus (Skip lesion)

non bloody poop

-noncaseaating granulomas/lymphoid aggs/cobblestoning of mucosa/creeping fat

-String sign

34
Q

Hirschsprung Dz

clinical presention

how do you diagnose it?

what causes it?

A

Defective relaxation of colon characterized by lack of ganglion cells/enteric nervous plexuses (Auerbach and Meissner)

-failure to pass meconium w/in 48 hrs / massive dilation megacolon

-rectal suction biopsy

-Failure of neural crest migration

35
Q

Angiodysplasia

A

Acquired malformation. Tortuous dilation of vessels

36
Q

Ischemic Colitis

where does it most often occur/ why?

A

Splenic Flexure & atherosclerosis of SMA

37
Q

Colonic Polyps

(Hyperplastic type)

what do they look like?

A

benignt, usually in the left colon (rectosigmoid)

saw tooth appearance on microscopy

38
Q

Colonic polyps

(adenomatous type)

what mutations cause this?

A

Neoplastic prolif of glands. pre-malignant

-mutations in APC and KRAS

39
Q

Familial Adenomatous polyposis (FAP)

whats the genetic description. what mutation

how do you treat it

A

Autosomal Dominant

  • mutation of the APC gene (chromosome 5)
  • colonectomy
40
Q

Gardner syndrome

A

FAP (familial adenomatous polyposis) + osteomas, fibromatosis (proliferation of fibroblasts)

41
Q

Turcot Syndrome

A

FAP + CNS Tumors (medulloblastoma and glial tumors)

42
Q

Juvenile polyposis syndrome

where?

A

Autosomal dominant syndrome in kids

consists of hamartomatous polyps in the

colon, stomach, small bowel

43
Q

Peutz-jaghers syndrome

what clinical signs would you see?

A

Autosomal dominant featuring shit ton of hamartomas throughout entire GI tract.

Hyperpigmented mouth, lips, hand, genetaila

increased risk of GI cancers

44
Q

Hereditary Non Polyposis Colorectal Carcinoma (HNPCC) / (Lynch syndrome)

which other cancers do it lead to?

A

Inherited mutation in the DNA mismatch repair genes

-microsatellite instability

-colorectal, endometrial, ovarian

45
Q

what does left-sided colon cancer look like?

A

Napkin ring lesion

pencil thin poop

46
Q

what does right sided colon cancer look like?

A

Iron deficiency anemia

47
Q

Whats CEA serum marker used for

A

Recurrent cancers