GI Neoplasia III: Carcinoid/GIST/Lymphomas: Tombazzi Flashcards

1
Q
Describe the 3 types of carcinoid tumors. 
Relative frequencies. 
Prognosis.
Mets
Clinical presentation
Other dz associations.
A

Types I and II most frequent (80%)
Type I- good prognosis, hypergastrinemia (antral origin)
Type II- some w/ mets. Gastrinoma (tumor outside stomach producing gastrin)
Type III- many w/ mets at Dx, aggressive. Not associated w/ hypergastrinemia.
Presentation: many asymptomatic, abd. pain, intermittent obstruction can occur.
Dz assoc: endocrine cell hyperplasia, autoimmune chronic atrophic gastritis, MEN-I, Z-E syndrome.

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2
Q

Describe the histology of neuroendocrine tumors.

A

Packets/nests of small, round cells that display salt and pepper chromatin. All neuroendocrine tumors looks the same, histologically, regardless of origin.

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3
Q

Most important prognostic factor for GI carcinoid tumors is:
Discuss the prognoses relative to this factor.

A

Location
Foregut (prox. to jejunum) rarely metastasize. Resection curative.
Midgut (jejunum, ileum) are often multiple and tend to be aggressive.
Hindgut (cecum, colorectum) found incidentally.

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4
Q

Describe the serological profile of autoimmune gastritis.

A

Abs to parietal cells (H+/K+ATPase, intrinsic factor)

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5
Q

Tx of Type I carcinoid tumor of antrum?

A

Remove antrum- curative, treats gastrinemia.

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6
Q

What immunostains are positive in Type II carcinoid tumor?

A

Chromogranin, synaptophysin, and CD56

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7
Q

Discuss the clinical presentation of carcinoid syndrome.

A

Episodes of cutaneous flushing, sweating, bronchospasm, colicky abdominal pain, diarrhea.
Right heart endocardial/valvular fibrosis (50%)
Pts can be overwhelmed by mass effect and hormones secreted into non-portal circulation (vasoactive peptides, serotonin, histamines)

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8
Q

What hormone do you expect to be highly elevated in Zollinger-Ellison (Z-E) syndrome?
How do you Dx Z-E using levels of this hormone?

A

:: Gastrin (>2000 pg/ml) w/ gastric pH 200 pg/ml is Dx. 83% sensitivity, 100% specificity.

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9
Q

Clinical presentation of Z-E syndrome:

A

Complicated peptic ulcer dz (secondary to excess gastric acid, thanks to excess gastrin release), diarrhea, abd. pain, weight loss, other.

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10
Q

How do you treat Z-E syndrome?

A

Surgical resection for solitary, non met. dz
Medical- high dose PPI, long acting octreotide
For mets: chemo, resection, embolization, radioablation, orthotopic liver transplant.

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11
Q

Two classic causes of hypertrophic gastritis:

A

Menetrier dz and Z-E syndrome

Menetrier- characteristic enlargement of gastric rugae in body and fundus (antrum not involved).
Z-E- Doubling of oxyntic mucosal thickness due to x5 number of parietal cells.

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12
Q

Describe the gastrointestinal stromal tumor (GIST).

A

Most common submucosal tumor of stomach.
From benign to very aggressive.
Behaves depending on size and histo
Most common manifestations: incidentally found GI bleeding, abd. mass, abd. pain.

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13
Q

Describe GIST histologically.

A

Arise from interstitial cells of Cajal (pacemaker cells)

Spindle-shaped or epithelioid, mesenchymal tumors.

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14
Q

Describe the mutation most commonly causing GIST.

A

95% of GIST pos. for RTK C-kit mutation, also DOG1

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15
Q

What is Carney triad?

A

non-hereditary syndrome of unknown etiology seen primarily in young females that includes:

  • Gastric GIST
  • Paraganglioma (extra-adrenal pheochromocytoma)
  • Pulm. chondroma
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16
Q

Tx for GIST:

A

Resection for local

RTK inhibitor for mets.

17
Q
Tell me about GI lymphoma. 
Where is it found?
Hodgkin or non-hodgkin?
B or T cells?
Presentation?
Dz associations?
A

Found in stomach and small bowel
Non-Hodgkin
B-cells
Same as adenocarcinoma. Epigastric pain, anorexia, weight loss, n/v, bleeding, early satiety.
H. pylori can cause MALT
Post-transplant lymphoproliferative due to Epstein-Barr Virus
Immunoproliferative small intestinal dz: malabsorption and Ig
Enteropathy assoc. T-Cell Lymphoma (EATCL): presents like celiac dz, but refractory to dietary changes.