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外阴丘疹性棘层松解性角化不良

Papular acantholytic dyskeratosis of the vulva.

作者信息

Sáenz Ana María, Cirocco Antonietta, Avendaño Mónica, González Francisco, Sardi José R

机构信息

Department of Dermatology, Hospital Universitario de Caracas, Luis Razetti School of Medicine, Caracas, Venezuela.

出版信息

Pediatr Dermatol. 2005 May-Jun;22(3):237-9. doi: 10.1111/j.1525-1470.2005.22312.x.

Abstract

We describe an 11-year-old girl with a persistent pruritic papular eruption on the vulva. Clinically, the lesions consisted of whitish papules and erosions located on the inner aspect of the labia majora. There was no familial history of skin diseases. Histologically, a biopsy specimen showed difuse hyperkeratosis, parakeratosis, acantholysis throughout the thickness of the epidermis, and the presence of corps ronds. Those findings were consistent with a diagnosis of acantholytic dyskeratosis. At 3 years follow-up, only isolated hyperkeratotic, asymptomatic papules on the same location remained. The occurrence of this focal and sporadic, localized form of acantholytic dyskeratosis seems to be rare in the pediatric population, as we could find no other child with this entity reported in the literature.

摘要

我们描述了一名11岁女童,其外阴出现持续性瘙痒性丘疹性皮疹。临床上,病变表现为位于大阴唇内侧的白色丘疹和糜烂。无皮肤疾病家族史。组织学上,活检标本显示弥漫性角化过度、角化不全、表皮全层棘层松解以及圆体细胞的存在。这些发现符合棘层松解性角化不良的诊断。随访3年时,同一部位仅残留孤立的角化过度、无症状丘疹。这种局限性、散发性、局部形式的棘层松解性角化不良在儿科人群中似乎很少见,因为我们在文献中未发现其他患有该疾病的儿童报道。

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