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色素性神经纤维瘤伴多毛症,与神经纤维瘤病无关。

Case of pigmented neurofibroma with hypertrichosis with no association to neurofibromatosis.

机构信息

Department of Dermatology, Chosun University, Gwangju, Korea.

出版信息

J Dermatol. 2009 Oct;36(10):541-4. doi: 10.1111/j.1346-8138.2009.00698.x.

Abstract

Pigmented neurofibroma (PNF) is a rare cutaneous tumor that has been observed in patients with or without neurofibromatosis (NF). This tumor is histologically characterized by the coexistence of scattered melanin-laden cells and benign spindle cells with neural differentiations. Hypertrichosis is the excessive growth of hair on non-androgen-dependent areas of the body. It has been reported that hypertrichosis may sometimes overlie a neurofibroma. We highlight a case of PNF with hypertrichosis on a 17-year-old woman with no associated NF. We also discuss the possible underlying pathogenic mechanism of a localized hypertrichosis in PNF patients.

摘要

色素性神经纤维瘤(PNF)是一种罕见的皮肤肿瘤,可见于有或无神经纤维瘤病(NF)的患者。该肿瘤在组织学上的特征是散在的含黑色素细胞和良性梭形细胞共存,并具有神经分化。多毛症是指身体非雄激素依赖部位的毛发过度生长。据报道,多毛症有时可能覆盖在神经纤维瘤上。我们报告了一例 17 岁女性患者的 PNF 合并多毛症,该患者无 NF 相关表现。我们还讨论了 PNF 患者局部性多毛症的潜在发病机制。

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