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一名患有朗格汉斯细胞组织细胞增多症的儿童出现获得性双侧聚集性斯皮茨痣。

Acquired bilateral agminated Spitz nevi in a child with Langerhans cell histiocytosis.

作者信息

Berk David R, Lane Alfred T

机构信息

Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.

出版信息

Pediatr Dermatol. 2010 May-Jun;27(3):282-4. doi: 10.1111/j.1525-1470.2010.01139.x.

Abstract

Multiple Spitz nevi are rare and may occur in agminated, widespread, or dermatomal distributions. Agminated Spitz nevi usually arise in children, presenting on grossly normal, hyperpigmented, or most rarely, hypopigmented skin. We present a child with Langerhans cell histiocytosis who developed bilateral agminated Spitz nevi in the inguinal area. Unusual features included the multifocal distribution, bilateral inguinal location, and co-occurrence with Langerhans cell histiocytosis.

摘要

多发性斯皮茨痣较为罕见,可呈簇状、广泛分布或沿皮节分布。簇状斯皮茨痣通常发生于儿童,表现于外观正常、色素沉着过度的皮肤,或极罕见地,表现于色素减退的皮肤。我们报告一例患有朗格汉斯细胞组织细胞增多症的儿童,其腹股沟区出现双侧簇状斯皮茨痣。不寻常的特征包括多灶性分布、双侧腹股沟部位以及与朗格汉斯细胞组织细胞增多症并存。

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