Acquired Bilateral Agminated Spitz Nevi in a Child with Langerhans Cell Histiocytosis
Acquired Bilateral Agminated Spitz Nevi in a Child with Langerhans Cell Histiocytosis
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患有朗格汉斯细胞组织细胞增多症的儿童获得性双侧斯皮茨痣
DOI：
10.1111/j.1525-1470.2010.01139.x
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发表时间：
2010
影响因子：
1.5
通讯作者：
A. Lane
中科院分区：
文献类型：
--
作者：
D. Berk;A. Lane
翻译后摘要：多发性斯皮茨痣是罕见的，可能会发生在聚集，广泛，或皮节分布。 发作性斯皮茨痣通常发生在儿童，表现为大体正常，色素沉着，或最罕见的，色素减退的皮肤。我们提出一个儿童郎格罕细胞组织细胞增生症谁开发双边集落斯皮茨痣在腹股沟区。不常见的特征包括多灶性分布、双侧腹股沟位置和与朗格汉斯细胞组织细胞增生症共发。
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.