GI Neoplasia III: Carcinoid/GIST/Lymphomas: Tombazzi Flashcards
Describe the 3 types of carcinoid tumors. Relative frequencies. Prognosis. Mets Clinical presentation Other dz associations.
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.
Describe the histology of neuroendocrine tumors.
Packets/nests of small, round cells that display salt and pepper chromatin. All neuroendocrine tumors looks the same, histologically, regardless of origin.
Most important prognostic factor for GI carcinoid tumors is:
Discuss the prognoses relative to this factor.
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.
Describe the serological profile of autoimmune gastritis.
Abs to parietal cells (H+/K+ATPase, intrinsic factor)
Tx of Type I carcinoid tumor of antrum?
Remove antrum- curative, treats gastrinemia.
What immunostains are positive in Type II carcinoid tumor?
Chromogranin, synaptophysin, and CD56
Discuss the clinical presentation of carcinoid syndrome.
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)
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?
:: Gastrin (>2000 pg/ml) w/ gastric pH 200 pg/ml is Dx. 83% sensitivity, 100% specificity.
Clinical presentation of Z-E syndrome:
Complicated peptic ulcer dz (secondary to excess gastric acid, thanks to excess gastrin release), diarrhea, abd. pain, weight loss, other.
How do you treat Z-E syndrome?
Surgical resection for solitary, non met. dz
Medical- high dose PPI, long acting octreotide
For mets: chemo, resection, embolization, radioablation, orthotopic liver transplant.
Two classic causes of hypertrophic gastritis:
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.
Describe the gastrointestinal stromal tumor (GIST).
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.
Describe GIST histologically.
Arise from interstitial cells of Cajal (pacemaker cells)
Spindle-shaped or epithelioid, mesenchymal tumors.
Describe the mutation most commonly causing GIST.
95% of GIST pos. for RTK C-kit mutation, also DOG1
What is Carney triad?
non-hereditary syndrome of unknown etiology seen primarily in young females that includes:
- Gastric GIST
- Paraganglioma (extra-adrenal pheochromocytoma)
- Pulm. chondroma