Shimotake T, Tokiwa K, Yanagihara J, Iwai N
Division of Surgery, Children's Research Hospital, Kyoto Prefectural University of Medicine, Japan.
Z Kinderchir. 1990 Aug;45(4):255-6. doi: 10.1055/s-2008-1042596.
We report on a 2-year-old male infant with accessory scrotum with lipoma presenting a perineal mass. Preoperatively no abnormality in the urinary tract and the anorectum was demonstrated. The tumour was resected and perineoplasty was performed. The resected specimen histologically revealed lipoma with tissue suggestive of scrotum. The patient recovered well and was discharged with no clinical complaints. This rare congenital anomaly is described in this paper. The slight continuity between the left scrotum and an accessory scrotal tissue in this case may suggest that this rare anomaly was derived from some abnormality in the migration of precursor tissue of scrotum.
我们报告一例2岁男性婴儿，患有伴有脂肪瘤的副阴囊，表现为会阴肿物。术前未发现尿路和直肠肛管有异常。切除肿瘤并进行了会阴成形术。切除标本的组织学检查显示为脂肪瘤，伴有提示阴囊的组织。患者恢复良好，出院时无临床不适。本文描述了这种罕见的先天性异常。本例中左侧阴囊与副阴囊组织之间的轻微连续性可能提示这种罕见异常源自阴囊前体组织迁移的某些异常。
