Kuraoka T, Taguchi K, Hosokawa S, Shimada K, Mori Y, Ikoma F, Uematsu K
Department of Urology, Hyogo College of Medicine.
Hinyokika Kiyo. 1994 Apr;40(4):361-3.
Testicular tumors derived from connective tissue, blood vessels and musculature are uncommon and intratesticular tumors of vascular origin are extremely rare. A rare case of capillary hemangioma of the testis in a child is reported. An 11-year-old boy was admitted with the chief complaint of painless mass in the right scrotum. He was diagnosed with a right testicular tumor by physical examination and ultrasonography, preoperatively. Right high orchiectomy was done on December 10, 1990. The testis measured 2.5 x 2.3 x 1.5 cm. Pathologically, the tumor was diagnosed as a capillary hemangioma of the testis.
源自结缔组织、血管和肌肉组织的睾丸肿瘤并不常见，而血管源性的睾丸内肿瘤极为罕见。本文报告了1例儿童睾丸毛细血管瘤的罕见病例。一名11岁男孩因右侧阴囊无痛性肿块为主诉入院。术前经体格检查和超声检查诊断为右侧睾丸肿瘤。1990年12月10日行右侧高位睾丸切除术。睾丸大小为2.5×2.3×1.5cm。病理检查诊断该肿瘤为睾丸毛细血管瘤。
