GI Neoplasia III Flashcards

1
Q

Put parietal cells, chief cells, and neuroendocrine cells in order of appearance from the bottom of a gastric gland to the top

A

Neuroendocrine cells are deepest in the gastric gland—- then Chief cells—-then Parietal cells near the top

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2
Q

What do parietal cells secrete ?

A

acid

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3
Q

What do chief cells secrete

A

Pepsin

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4
Q

Pathophysiology of carcinoid tumor

A

Chronic gastritis or gastric acid suppression can lead to hypergastrinemia (high gastrin levels trying to stimulate more acid release)

This in turn can lead to gastric diffuse neuroendocrine hyperplasia which can develop into a gastric carcinoid tumor

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5
Q

What stains are used to insure that a tumor is neuroendocrine in nature?

A

CHROMOGRANIN and somatrophysin

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6
Q

What is type I carcinoid syndrome?

A

Tumor is associated with hypergastrinemia, usuallyindolent (slow growing), and mets are very uncommon

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7
Q

What is type II carcinoid syndrome?

A

Tumor is associated with high gastrin levels that are coming from outside the stomach (usually a pancreatic tumor or something of that sort). Treat the carcinoid syndrome but also treat the tumor

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8
Q

Type III carcinoid syndrome?

A

Not associated with hypergastrinemia, very aggressive, many with metastases at diagnosis, assoc with carcinoid syndrome

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9
Q

ANd what does carcinoid syndrome look like

A

bunch of nodules in the fundus of the stomach

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10
Q

What are the possible ways to treat a type 1 carcinoid tumor?

A
  • take out the nodules

- take out the antrum of the stomach where the gastrin is coming from

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11
Q

Zollinger Ellison Syndrome

A

High levels of gastrin due to a gastrin secreting tumor in the pancreas or small intestine usually.

Diagnosis made bby gastrin level over 1,000 with gastrin pH below 5

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12
Q

Treatment of zollinger-ellison syndrome

A
  • surgical resection
  • High dose PPI
  • Long acting somatostatin analog
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13
Q

Outside of the stomach, what is the most common site of a carcinoid tumor

A

small bowel

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14
Q

Where in the small intestine do carcinoid tumors generally appear?

A

Illeum and appendix

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15
Q

What age range for intestinal carcinoid tumors

A

late middle age

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16
Q

most common symptom of intestinal carcinoid tumor?

A

abdominal pain

17
Q

Carcinoid syndrome is characterized by

A

bronchospasm, diarrhea, flushing of skin

18
Q

Carcinoid heart disease

A

right hear endocardial fibrosis

19
Q

What kind of carcinoid tumors generally lead to carcinoid syndrome?

A

carcinoid tumors in the ileum that have liver mets

20
Q

What causes carcinoid syndrome symptoms

A

vasoactive polypeptides and serotonin levels

21
Q

What test is diagnostic?

A

High urine 5-hydroxyindole acetic acid

22
Q

Colorectal neuroendocrine umors most commonly seen where

A

right colon, usually a large mass

23
Q

Gastrointestinal stromal tumor generally presents in what way

A

incidental finding….unless they are symptomatic (i.e have black tarry stool)

24
Q

Gastrointestinal stromal tumors most common where?

A

stomach and small intestine

25
Q

GIST derive from what?

A

Cells of cajal, GI pacemaker cells that form the interface between autonomic innervation and smooth muscle cells of the gut

26
Q

GIST stains positive for

A

CD117

27
Q

Most GISTs have a mutation in what?

A

KIT transmembrane receptor

28
Q

DXof GIST

A

CT detects them but be careful with endoscopy because it may come back false negative since they are in the wall and not the mucosa

Endoscopic ultrasound guided fine needle aspiration is best test

29
Q

Post- transplant lymphoproliferative disorder?

A

Immunosuppresion allows B cells with EBV to proliferate in an uncontrolled manner

30
Q

DX of PTLD

A

blood test for EBV DNA

31
Q

GI lymphoma

A

70% in stomach

32
Q

look at GI lymphoma stuff

A

ok