Hattori Ryo, Kubo Tateki, Yano Kenji, Tanemura Atsushi, Yamaguchi Yuji, Itami Satoshi, Hosokawa Ko
Department of Plastic Surgery, Osaka University Graduate School of Medicine, Suita-shi, Japan.
Dermatol Surg. 2003 Oct;29(10):1071-2. doi: 10.1046/j.1524-4725.2003.29306.x.
Nevus lipomatosus cutaneous superficialis (NLCS) is a relatively rare condition. Although NLCS can affect any region of the entire body, no case of NLCS in the clitoris has ever been reported.
To report a case of NLCS of the clitoris that presented manifestations that were similar to female pseudohermaphrodism.
This is a case report and review of the literature.
A congenital, soft, skin-colored lesion of the clitoris in a 1-year-old girl resembled female pseudohermaphrodism. It was resected, and the histologic diagnosis was NLCS. Postoperatively, there was no subsequent change in the lesion during the 3-year follow-up period.
We reported a case of congenital solitary NLCS of the clitoris. Although NLCS might be a relatively rare condition, we should consider it in the differential diagnosis of female pseudohermaphrodism.
浅表性皮肤脂肪瘤样痣（NLCS）是一种相对罕见的病症。尽管NLCS可累及全身任何部位，但从未有过阴蒂发生NLCS的病例报道。
报告1例表现类似于女性假两性畸形的阴蒂NLCS病例。
这是1例病例报告及文献复习。
1名1岁女童阴蒂出现先天性、质地柔软、肤色的病变，类似女性假两性畸形。病变被切除，组织学诊断为NLCS。术后，在3年随访期内病变无后续变化。
我们报告了1例先天性孤立性阴蒂NLCS病例。尽管NLCS可能相对罕见，但在女性假两性畸形的鉴别诊断中应考虑到该病。
