Clinical Pathology · MU Sofia

77. Benign gastric tumors – of epithelial and mesenchyme origin. Stromal tumors – GIST.

Covers benign gastric tumours of epithelial and mesenchymal origin, taking gastric polyps, fundic gland polyps, gastric adenoma, lipomas and leiomyomas in turn, then the potentially malignant carcinoid tumour and gastrointestinal stromal tumour. Includes a classification of polyp types, a note on carcinoid location as the main prognostic factor, GIST histology and KIT mutation, and a reminder of immunohistochemical markers, cell of origin and imatinib response, with a labelled micrograph of a spindle-cell GIST.

Inside: 1 section · 1 labelled picture · 16 flashcards · 3 min

Topic 77 of 138 in the MU Sofia syllabus for Clinical Pathology (Medicine, Year 4). The free AceMed note covers it in 1 section, about 515 words (3 min of reading), with 16 flashcards.

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  1. Benign gastric tumors - of epithelial and mesenchymal origin. Stromal tumors - GIST

Benign gastric tumors - of epithelial and mesenchymal origin. Stromal tumors - GIST

The list of benign gastric tumors is:

  • Gastric polyps
  • Fundic gland polyps
  • Gastric adenoma
  • Lipomas
  • Leiomyomas

Two potentially malignant ones are:

  • Carcinoid tumour
  • Gastrointestinal stromal tumor (GIST)

Gastric polyps (epithelial tumour)

  • These are nodules or masses that project above the mucosa
  • May be as a result of hyperplasia, inflammation, ectopia or neoplasia
  • There are different types of polyps
  • Inflammatory and hyperplastic polyps
  • Most common by far, affect those 50-60
  • Usually have chronic gastritis with H.pylori
  • Frequently multiple, stable, smooth, ovoid and less than 1cm
  • Microscopically polyps have irregular, cystically dilated foveolar glands and lamina propria is edematous
  • Polyps larger than 1.5cm have increase risk of dysplasia, a precancerous in situ lesion
  • Fundic gland polyps
  • Sporadic and in persons with familial adenomatous polyposis (FAP)
  • No neoplastic potential
  • Occur as a result of proton pump inhibitor use
  • May be asymptomatic, or cause vomiting and nausea
  • Gastric adenoma
  • 10% of cases, occur in background of chronic gastritis with atrophy
  • Risk of adenocarcinoma development, bigger polyp, bigger risk
  • (see gastric adenoma section below)

Gastric lipoma (mesenchymal tumour)

  • Derived from fat tissue, they are rare (less than 1% of gastric neoplasms)
  • May present with upper GI bleeding, dyspepsia or gastric obstruction
  • Histology shows adipose cells with fibrous capsule

Gastric Leiomyoma (mesenchymal tumour)

  • Rare, asymptomatic, generally found incidentally
  • Derived from smooth muscle of muscularis propria or lamina muscularis mucosa of stomach

Carcinoid tumour (neuroendocrine tumour)

  • Of neuroendocrine origins (neuroendocrine cells of the gut mucosa)
  • Most are asymptomatic however all have malignant potential and about 10% secrete hormones (most commonly serotonin, causing flushing, diarrhea, wheezing, abdominal cramps and peripheral edema).
  • In the GI system, Carcinoid tumours are most common in the appendix or small intestines.
  • Known as carcinoid as they are slower growing than carcinomas
  • They created small yellow polypoid lesions that can cause kinking of bowel and obstruction. Histologically the are composed of islets, strands and glands.
  • The most important prognostic factor is the location
  • Foregut - stomach + proximal duodenum rarely metastasize and are cured by resection
  • Midgut - jejunum + ileum tend to be more aggressive
  • Hind gut - appendix and colorectum - almost always benign, although rectal forms generally produce polypeptide hormones

Gastrointestinal stromal tumour (GIST) (mesenchymal tumour)

  • Most common mesenchymal tumour of the abdomen, more than half in the stomach
  • More common in males - 80% have mutation of tyrosine kinase c-KIT gene

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