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伴有组织细胞样浸润和中性粒细胞减少的Sweet综合征:一种罕见的组合。

Sweet syndrome with histiocytoid infiltrate and neutropenia: a rare combination.

作者信息

Liu Chuan-I, Hsiao Cheng-Hsiang, Wu June-Tai, Tsai Tsen-Fang

机构信息

Department of Dermatology, Cathay General Hospital, Taipei, Taiwan.

出版信息

J Am Acad Dermatol. 2009 Nov;61(5):882-4. doi: 10.1016/j.jaad.2008.12.038. Epub 2009 Sep 6.

Abstract

Histiocytoid Sweet syndrome is a recently described variant of acute febrile neutrophilic dermatosis. The histiocytoid cells are easily misinterpreted as histiocytes, when in fact they are immature myeloid cells. The recognition of myeloperoxidase expression in these cells is important in avoiding confusion with histiocyte-rich dermatoses. Herein, we report a case of histiocytoid Sweet syndrome with neutropenia that had an unusual presentation. The recognition of this rare combination helps expand the spectrum of Sweet syndrome with histiocytoid infiltrate.

摘要

组织细胞样Sweet综合征是急性发热性嗜中性皮病的一种最近描述的变体。组织细胞样细胞很容易被误解为组织细胞,而实际上它们是未成熟的髓细胞。认识到这些细胞中髓过氧化物酶的表达对于避免与富含组织细胞的皮肤病混淆很重要。在此,我们报告一例伴有中性粒细胞减少症的组织细胞样Sweet综合征病例,该病例有不寻常的表现。认识到这种罕见的组合有助于扩大伴有组织细胞样浸润的Sweet综合征的范围。

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