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斯威特综合征:11例病例的回顾性临床、组织病理学及免疫组织化学分析

Sweet's syndrome: a retrospective clinical, histopathological and immunohistochemical analysis of 11 cases.

作者信息

Corazza Monica, Lauriola Maria Michela, Borghi Alessandro, Marzola Andrea, Virgili Annarosa

机构信息

Department of Clinical and Experimental Medicine, Section of Dermatology, University of Ferrara, Ferrara, Italy.

出版信息

Acta Derm Venereol. 2008;88(6):601-6. doi: 10.2340/00015555-0526.

Abstract

The aim of this paper is to report our clinical experience of Sweet's syndrome, a severe dermatological disease which may be extremely important to recognize for the early diagnosis of a neoplastic disorder. Eleven patients affected by Sweet's syndrome, treated at the Department of Dermatology, University of Ferrara, Ferrara, Italy, during 1998 to 2004, were evaluated. A retrospective analysis was performed. Data on age, sex distribution, clinical data, histopathological and immunohistochemical findings and therapy were collected. We observed one patient with idiopathic form, 5 patients affected by the para-inflammatory variant and 5 para-neoplastic cases (with haemoproliferative diseases). The cases with the para-inflammatory form were affected by minor infectious manifestations. Prolonged follow-up is necessary to verify that a case of idiopathic variant is not really a paraneoplastic form. Based on immunohistochemical analysis, we cannot exclude that true histiocytes, immunoreactive for CD68/PGM, infiltrate the dermis in Sweet's syndrome lesions.

摘要

本文旨在报告我们关于Sweet综合征的临床经验。Sweet综合征是一种严重的皮肤病,对于肿瘤性疾病的早期诊断而言,认识它可能极其重要。我们评估了1998年至2004年期间在意大利费拉拉大学皮肤科接受治疗的11例Sweet综合征患者。进行了回顾性分析。收集了有关年龄、性别分布、临床数据、组织病理学和免疫组化结果以及治疗方面的数据。我们观察到1例特发性形式的患者、5例受副炎症性变体影响的患者以及5例副肿瘤性病例(伴有血液增殖性疾病)。副炎症性形式的病例伴有轻微感染表现。需要进行长期随访以证实特发性变体病例并非真正的副肿瘤性形式。基于免疫组化分析,我们不能排除真正的组织细胞(对CD68/PGM呈免疫反应性)浸润Sweet综合征皮损真皮层的可能性。

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