Katsuno S, Hibi H, Takashi M, Yamamoto M, Miyake K, Sakata T
Department of Urology, Nagoya University School of Medicine.
Hinyokika Kiyo. 1996 Oct;42(10):751-4.
Liposarcomas in the scrotum are relatively rare and only 40 cases have previously been reported in Japan. The inside wall of the scrotum is an unusual origin and we report here two cases arising at this site that have been followed for 21 and 40 months, respectively, after surgical resection. Case 1: the patient was a 24-year-old male who noticed a left intrascrotal mass which was histologically demonstrated to be a myxoid type liposarcoma. Case 2: the patient was a 66-year-old male who had the complaint of a left intrascrotal swelling. He underwent radical orchiectomy and histologic examination of the resected tumor revealed a well-differentiated type of liposarcoma. These two cases are the 41st and 42nd intrascrotal liposarcomas reported in Japan.
阴囊脂肪肉瘤相对罕见,日本此前仅报告过40例。阴囊内壁是一个不寻常的发病部位,我们在此报告两例起源于此部位的病例,分别在手术切除后随访了21个月和40个月。病例1:患者为一名24岁男性,发现左侧阴囊内有一肿块,组织学检查显示为黏液样型脂肪肉瘤。病例2:患者为一名66岁男性,主诉左侧阴囊肿胀。他接受了根治性睾丸切除术,切除肿瘤的组织学检查显示为高分化型脂肪肉瘤。这两例是日本报告的第41例和第42例阴囊脂肪肉瘤。