X-linked incontinentia pigmenti or Bloch-Sulzberger syndrome: a case report

被引：7

作者：

Pereira, Marcela A. C. ^{[1
]}

Mesquita, Lismary A. de F. ^{[2
]}

Budel, Anelise R. ^{[3
]}

Cabral, Carolina S. P. ^{[4
]}

Feltrim, Amanda de S. ^{[4
]}

机构：

[1] Hosp Univ Evangel Curitiba, Curitiba, Parana, Brazil

[2] Hosp Santa Casa de Misericordia Curitiba, Curitiba, Parana, Brazil

[3] Fac Evangel Med Curitiba, Disciplina Dermatol, Curitiba, Parana, Brazil

[4] Fac Evangel Parana, Curitiba, Parana, Brazil

来源：

ANAIS BRASILEIROS DE DERMATOLOGIA | 2010年 / 85卷 / 03期

关键词：

Genetics; Incontinentia pigmenti; X chromosome;

D O I：

10.1590/S0365-05962010000300013

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100227 [皮肤病学];

摘要：

Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonates. Skin manifestations are the most common and occur in four quite distinct phases. A female infant presented vesiculobullous lesions on trunk and limbs, and a verrucous lesion on the right palm. Biopsy revealed eosinophil exocytosis and pigment incontinence, confirming the clinical hypothesis. Although uncommon, incontinentia pigmenti should be taken into consideration as a possible differential diagnosis when vesiculobullous and verrucous lesions are present in childhood.

引用

页码：372 / 375

页数：4

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