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复合性蓝色痣:基因组时代概念的再评价。

Compound blue nevus: a reappraisal of the concept in the genomic era.

机构信息

Department of Biopathology, Center Léon Bérard, 28, Rue Laennec, 69008, Lyon, France.

Department of Laboratory Medicine, Service clinique d'anatomopathologie, CHU de Québec-Université Laval, Quebec, Canada.

出版信息

Virchows Arch. 2020 Mar;476(3):439-443. doi: 10.1007/s00428-019-02667-w. Epub 2019 Nov 21.

Abstract

We report a series of 21 compound blue nevi, a rare variant in the vast clinical and morphological spectrum of blue melanocytic proliferations. Clinically, they presented in young adults, with a slight female predominance. One-third were located on the dorsum of the foot. Morphologically, all cases displayed large dendritic melanocytes restricted to the deep layers of the epidermis. The compound component was central and evenly distributed. Melanocytic density ranged from scarce isolated cells to a confluent lentiginous architecture. In 12 of the 21 cases, junctional nests of small, bland, weakly pigmented melanocytes were associated. These nests became confluent in the most cellular cases. In all cases, a dermal component was immediately present underneath, mainly of cellular blue nevus-type. All cases were genetically confirmed to harbor either a GNAQ or GNA11 hotspot mutation. This study expands the morphological spectrum of blue nevi that should not be restricted to a strictly intradermal melanocytic proliferation.

摘要

我们报告了一系列 21 例复合蓝色痣,这是蓝色黑素细胞增生在广泛的临床和形态学谱中的罕见变体。临床上,它们发生在年轻人中,略偏向女性。三分之一位于足背部。形态上,所有病例均显示局限于表皮深层的大型树枝状黑素细胞。复合成分位于中央且均匀分布。黑素细胞密度从稀少的孤立细胞到融合性的雀斑样结构不等。在 21 例中的 12 例中,存在与小而温和、色素沉着弱的交界性巢相关的小而温和、色素沉着弱的交界性巢。在最具细胞性的病例中,这些巢融合在一起。在所有病例中,下方立即存在真皮成分,主要为细胞性蓝色痣样。所有病例均经基因证实存在 GNAQ 或 GNA11 热点突变。本研究扩展了蓝色痣的形态学谱,不应仅限于严格的真皮内黑素细胞增生。

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