阴蒂浅表性脂肪瘤样痣。
Nevus lipomatosus cutaneous superficialis of the clitoris.
作者信息
Hattori Ryo, Kubo Tateki, Yano Kenji, Tanemura Atsushi, Yamaguchi Yuji, Itami Satoshi, Hosokawa Ko
机构信息
Department of Plastic Surgery, Osaka University Graduate School of Medicine, Suita-shi, Japan.
出版信息
Dermatol Surg. 2003 Oct;29(10):1071-2. doi: 10.1046/j.1524-4725.2003.29306.x.
BACKGROUND
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.
OBJECTIVE
To report a case of NLCS of the clitoris that presented manifestations that were similar to female pseudohermaphrodism.
METHODS
This is a case report and review of the literature.
RESULTS
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.
CONCLUSION
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.
背景
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。
目的
报告1例表现类似于女性假两性畸形的阴蒂NLCS病例。
方法
这是1例病例报告及文献复习。
结果
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。
结论
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。
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