Ito Timothy, Melamed Jonathan, Perle Mary Ann, Alukal Joseph
Fox Chase Cancer Center Philadelphia, PA.
Department of Pathology, New York University School of Medicine New York, NY.
Am J Clin Exp Urol. 2015 Apr 25;3(1):43-7. eCollection 2015.
Clear cell sarcoma of the penis is exceedingly rare with only one prior case involving the penis reported in the literature. We present the case of a 32 year old male who presented with an infiltrative neoplasm at the base of the penis as well as extensive metastatic disease to the lymph nodes and bone. Morphologic, immunohistochemical and cytogenetic findings established the diagnosis of clear cell sarcoma. Despite chemotherapy the patient's disease was rapidly progressive and the patient died of disease within 8 months of diagnosis.
阴茎透明细胞肉瘤极为罕见，文献中仅报道过一例累及阴茎的病例。我们报告一例32岁男性患者，其阴茎根部出现浸润性肿瘤，并伴有广泛的淋巴结和骨转移。形态学、免疫组化和细胞遗传学检查结果确诊为透明细胞肉瘤。尽管进行了化疗，患者病情仍迅速进展，确诊后8个月内死于该疾病。
