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急性发热性嗜中性皮病。37例患者的组织病理学研究及文献复习。

Acute febrile neutrophilic dermatosis. A histopathological study of 37 patients and a review of the literature.

作者信息

Jordaan H F

机构信息

Department of Dermatology, Tygerberg Hospital, Republic of South Africa.

出版信息

Am J Dermatopathol. 1989 Apr;11(2):99-111.

PMID:2653084
Abstract

More than 100 cases of acute febrile neutrophilic dermatosis (AFND) have been documented since the original description by Sweet in 1964. Review articles have focused on clinical features. The present study documents the histopathological features of 54 biopsies obtained from 37 patients with early AFND. All patients fulfilled the criteria for the diagnosis of AFND as suggested by Su and Liu. Macular, papulonodular and scaly, annular, or arciform lesions are represented, histopathologically by lymphocytic, predominantly neutrophilic, and mixed infiltrates with a prominent histiocytic component. Characteristic histopathology--i.e., a pale, edematous epidermis, subepidermal edema with extravasated red cells, and a more or less diffuse infiltrate of mature neutrophilis in the upper dermis without vasculitis--is only found during the neutrophilic phase. This is an important consideration when evaluating sections of patients with possible AFND. AFND is a disease that represents a wide spectrum of clinical and histological features. Implications regarding differential diagnoses are discussed.

摘要

自1964年斯威特首次描述急性发热性嗜中性皮病(AFND)以来,已有100多例病例被记录在案。综述文章主要关注临床特征。本研究记录了从37例早期AFND患者身上获取的54份活检组织的组织病理学特征。所有患者均符合苏和刘提出的AFND诊断标准。斑疹、丘疹结节状、鳞屑状、环状或弧形病变在组织病理学上表现为淋巴细胞浸润,主要为嗜中性粒细胞浸润,以及伴有显著组织细胞成分的混合浸润。特征性组织病理学表现——即苍白、水肿的表皮,伴有红细胞外渗的表皮下水肿,以及真皮上层或多或少弥漫性的成熟嗜中性粒细胞浸润且无血管炎——仅在嗜中性粒细胞阶段出现。在评估可能患有AFND的患者切片时,这是一个重要的考虑因素。AFND是一种具有广泛临床和组织学特征的疾病。文中讨论了其在鉴别诊断方面的意义。

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