Marzano Angelo V, Ramoni Stefano, Caputo Ruggero
Institute of Dermatological Sciences, University of Milan - Fondazione IRCCS, Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Milan, Italy.
Dermatology. 2008;216(4):305-11. doi: 10.1159/000113942. Epub 2008 Jan 29.
Amicrobial pustulosis of the folds (APF) is a rare entity characterized by relapsing pustular lesions involving mainly the cutaneous folds. The disease typically occurs in the context of an autoimmune disorder and is classified within the spectrum of neutrophilic dermatoses.
We studied 6 young females having APF associated with various autoimmune diseases or with the presence of serum autoantibodies and reviewed the literature, in order to give a clinical overview on this syndrome.
Various routine and immunological laboratory tests, histopathological examination as well as direct and indirect immunofluorescence examinations were performed. In vitro neutrophil function was evaluated in 5 cases. We report our findings and compare our cases with those published in the literature.
Clinically, at least one major fold and at least one minor fold as well as the anogenital area were always involved. We documented an impaired neutrophil chemotaxis in 2 subjects, neutrophil dysfunction, thus failing to be a verifying criterion.
APF is a neutrophilic dermatosis affecting young females, which usually shows a benign clinical behavior. Although systemic corticosteroids are the most widely used therapeutic agents, we suggest that the combination of cimetidine and ascorbic acid represents a safe alternative, which may induce long-lasting clinical remission.
皱褶部无菌性脓疱病(APF)是一种罕见疾病,其特征为复发性脓疱性损害,主要累及皮肤皱褶部位。该病通常发生于自身免疫性疾病背景下,属于嗜中性皮病范畴。
我们研究了6例与各种自身免疫性疾病相关或存在血清自身抗体的APF年轻女性患者,并复习文献,以对该综合征进行临床概述。
进行了各种常规和免疫学实验室检查、组织病理学检查以及直接和间接免疫荧光检查。对5例患者评估了体外中性粒细胞功能。我们报告研究结果,并将我们的病例与文献报道的病例进行比较。
临床上,至少一个主要皱褶部位、至少一个次要皱褶部位以及肛门生殖器区域总是受累。我们记录到2例患者中性粒细胞趋化功能受损,中性粒细胞功能障碍因此未能成为一个验证标准。
APF是一种累及年轻女性的嗜中性皮病,通常表现为良性临床过程。虽然全身用皮质类固醇是最广泛使用的治疗药物,但我们建议西咪替丁和维生素C联合使用是一种安全的替代方法,可能诱导长期临床缓解。