gastrointestinal stromal tumor of the abdominal soft tissue
Monday 12 September 2011
Gastrointestinal stromal tumor (GIST) typically occurs in the gastrointestinal (GI) tract, and expresses KIT protein that is associated with KIT or platelet-derived growth factor receptor-α (PDGFRA) gene mutation.
not otherwise specified regions of the abdominal cavity.
size from 4 to 33 cm (median, 15 cm) in maximum diameter
relatively low mitotic counts (median, 3.5 per 50 high-power fields)
Morphologically, most cases are of epithelioid cell or mixed epithelioid and spindle cell type, accompanied by variable amounts of myxoid stroma.
protein kinase C (PKC) θ (90%)
discovered on GIST-1 (DOG1) (90%)
negative for KIT (0%).
The majority of the examined cases (78%) have PDGFRA mutations in exon 12 or exon 18.
Rare cases (11%) have a mutation in KIT exon 11.
Very rare cases have no mutation in either KIT or PDGFRA.
KIT-negative EGISTs can be characterized by preferential omental origin, epithelioid cell type, low mitotic activity, and mutation of the PDGFRA gene, and these features are similar to those of KIT-negative gastric GISTs.
As KIT-negative EGISTs should be considered to be a potential abdominal soft tissue neoplasm, immunohistochemical staining panel and molecular analysis are necessary not only to confirm the diagnosis but also to determine the therapeutic strategy.
KIT-Negative Gastrointestinal Stromal Tumor of the Abdominal Soft Tissue: A Clinicopathologic and Genetic Study of 10 Cases. Yamamoto H, Kojima A, Nagata S, Tomita Y, Takahashi S, Oda Y. Am J Surg Pathol. 2011 Sep;35(9):1287-95. PMID: 21836495