Özet:

Alveolar soft part sarcoma is a rare, distinctive sarcoma most frequently encountered in patients 15-35 years of age, and typically located in the deep soft tissues of the lower extremities in adults. If the tumor affects infants and children, it is often located in the head and neck region. This uncommon neoplasm presents as a slowly growing, painless mass. Because of relative lack of symptoms, it could be easily overlooked and frequent late metastases might be seen at the time of diagnosis after a prolonged clinical course. Herein, we an alveolar soft part sarcoma case occurred in a 64 year old male patient with the complaint of a slowly growing mass on his right glutea. The operation specimen was a poorly circumscribed soft tissue and cut section was gray-white with areas of hemorrhage and necrosis. On light microscopic investigation, the histological picture reminiscent of alveolar soft part sarcoma with cells tumoral lesion in an organoid patern, and malignant melanoma like morphology somewhere in the tumor were observed. Immunohistochemical staining revealed position with vimentin, S-100, EMA, Pankeratin and CD68, but negativity with HMB 45, Melan A, CD 10, sinaptofisin and chromogranin A in the tumor cells. Although immuno-histochemical findings were not specific, the histopatho-logical picture was appropriate for the diagnosis. In conclusion, despite the relatively slow growth, the ultimate prognosis is poor so it is very important to recognize this malignant injury with an unexpected clinical presentation and distinct immunohistomorphological features exist.

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