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儿童Sweet综合征的罕见病例:与持久性隆起性红斑的重叠表现。

An unusual case of Sweet syndrome in a child: overlapping presentation with erythema elevatum diutinum.

作者信息

Wang Tingting, Liu Hongjie, Wang Lin, Guo Zaipei, Li Li

机构信息

Department of Dermatovenereology, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Am J Dermatopathol. 2014 Jun;36(6):e114-6. doi: 10.1097/DAD.0000000000000026.

Abstract

In 1964, Sweet described an acute febrile neutrophilic dermatosis. It is now widely accepted that Sweet syndrome is one of the associated neutrophilic dermatoses. Herein, we describe an unusual case of Sweet syndrome in a 5-year-old child who suffered from recurrent papules, plaques, and blisters on his face and trunk after the initial onset of fever without an obvious cause. Two skin biopsies were performed. The histopathological findings of the left arm biopsy showed a subepidermal blister with dense infiltrating neutrophils within the blister that were superficial to the middle layer of the dermis. The biopsy from a plaque on the left leg showed a dense infiltrate of neutrophils and a large number of infiltrating histiocytes superficial to the middle layer of the dermis. Direct immunofluorescence of a skin biopsy from the left arm confirmed that immunoglobulin M (IgM), IgG, IgA, and C3 expression were negative.

摘要

1964年,斯威特描述了一种急性发热性嗜中性皮病。如今,斯威特综合征是相关嗜中性皮病之一已被广泛接受。在此,我们描述了一例不寻常的斯威特综合征病例,一名5岁儿童在无明显诱因发热初起后,面部和躯干反复出现丘疹、斑块和水疱。进行了两次皮肤活检。左臂活检的组织病理学结果显示表皮下疱,疱内有密集浸润的嗜中性粒细胞,位于真皮中层浅层。左腿斑块的活检显示真皮中层浅层有密集的嗜中性粒细胞浸润和大量浸润的组织细胞。左臂皮肤活检的直接免疫荧光证实免疫球蛋白M(IgM)、IgG、IgA和C3表达均为阴性。

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