A gastrointestinal stromal tumor (GIST) masquerading as an ovarian mass
© Carlomagno and Beneduce; licensee BioMed Central Ltd. 2004
Received: 18 February 2004
Accepted: 13 May 2004
Published: 13 May 2004
Malignant gastrointestinal stromal tumors (GIST) are rare mesenchymal tumors originating in the wall of the gastrointestinal tract. Myogenic gastrointestinal stromal tumor, a distinctive morphologic variant is characterized by an unusually prominent myxoid stromal background.
We report a case of myxoid variant of GIST in a 42 years old woman presenting as an epigastric mass associated to an ovarian cyst and elevated CA-125. Histologically, the lesions was composed of a proliferation of spindle cells in an abundant myxoid stroma, without evidence of atypia or anaplasia. Immunohistochemical stains showed strong positive staining with muscle actin, positive staining with CD34 and weak positive staining with CD117, while showed negative for S-100.
At surgery every effort should be made to identify the origin of the tumor. A complete surgical removal of the tumor should be obtained, as this is the only established treatment that offers long term survival.
KeywordsGastrointestinal stromal tumors GIST ovarian neoplasm
Gastrointestinal stromal tumors (GIST) are rare tumors that may arise anywhere in the tubular gastrointestinal tract, but stomach is the most common site of localization. Surgery is the main stay of treatment and complete resection is achieved in most of cases . The 5 year overall survival ranges from 21% to 88% in different series, depending from risk grading and completeness of surgical resection [1–4]. In light of the tendency of these tumors to pursue an indolent clinical course with a significant risk of late relapse, a brisk follow-up is advocated for all patients . Imatinib mesylate is proposed as therapy for high risk GISTs after surgery . A distinctive morphologic variant of gastrointestinal stromal tumor has been described, characterized by a prominent myxoid stromal background reminiscent of a neural neoplasm but lacking the immunohistochemical or ultrastructural features of peripheral nerve sheath or ganglionic differentiation. This variant is more frequent in women and mostly occurs in the stomach. These lesions are described grossly as well circumscribed, unencapsulated, with a prominently myxoid and often cystic cut surface . We report a case of myxoid variant GIST, occurring in a 42 year old woman.
Fletcher et al.,  classified these tumors in to very low, low, intermediate and high risk, categories according to tumor size and mitotic count. Tumors <2 cm and mitotic count <5/50 high power field (HPF) were categorized as very low risk; tumor size 2–5 cm and mitotic count <5/50 HPF as low risk; tumor size <5 cm and mitotic count 6–10/50 HPF or tumor size 5–10 cm and mitotic count <5/50 HPF as intermediate risk; tumor size >5 cm and mitotic count >5/50 HPF or tumor size >10 cm and any mitotic rate or tumor any size and mitotic rate >10/50 HPF as high risk. As reported by others [8–10], GIST may mimic a pelvic masses. In such circumstances they are first noticed by gynecologists and are often diagnosed, prior to surgery, as ovarian tumors, either as metastatic from, or metastatizing to gastrointestinal tract. Only at surgery their nature is fully understood. The same was true in our case as a solid epigastric mass was associated to an ovarian cystic lesion similar to that in Krukenberg tumor. Therefore, in presence of a pelvic mass, especially if other unusual signs are present, the possibility of other than a gynecologic tumor has to be considered. At surgery, every effort should be made to identify the origin of the tumor and related anatomic structures. In the case of GIST, a complete surgical removal of the tumor should be obtained, as despite significant advances in new chemotherapic regimens have been radical surgical removal only offers chance of long term survival.
Written consent was obtained from the patient or their relative for publication of study.
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