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[银屑病合并严重毁形性银屑病关节炎。临床病例及文献综述]

[Psoriasis complicated with severe mutilating psoriatic osteoarthropathy. Clinical case and review of the literature].

作者信息

Iannello S, Camuto M, Cavaleri A, Fagone S, Belfiore F

机构信息

Istituto di Medicina Interna e Specialità Internistiche, Cattedra di Medicina Interna, Ospedale Garibaldi, Università degli Studi, Catania.

出版信息

Minerva Med. 2000 Sep;91(9):191-226.

Abstract

Aim of this paper is to discuss, on the basis of an extensive critical review of the recent literature, the case of a 56-yr-old male patient who suffered from cutaneous psoriasis and psoriatic arthritis mutilans (PA) (polyarticular, symmetric, destruent and erosive) with involvement of the hands, feet and spine, associated with android obesity and mild type 2 diabetes mellitus. HLA typing of the patient showed the HLA-A3-Ax, B14-B63 and Cw4-Cw6 haplotypes, some of which are associated or correlated with susceptibility to PA. Cutaneous psoriasis is a chronic inflammatory dermatitis, with onset at any age and affecting approximately 2% of the western populations. In 5-7% of patients, it is associated with articular manifestations or true arthritis. PA is a chronic, inflammatory, seronegative arthropathy which may develop in some psoriasis patients, may involve peripheral and axial (spondarthritis) joints and may lead to severe joint destruction. Genetic, immunologic and environmental (i.e., infectious agents or trauma) factors seem to play an important role in the onset and clinical appearance of PA. Although PA is a clinically monomorphic disease, it may show different heterogenous subgroups with differences in their etiopathogenesis. When PA is suspected, it is mandatory to analyze carefully the patient's familiar history, search attentively for the specific skin features, exclude a septic arthritis (especially if the involvement is monoarticular) and, in the cases of fulminant disease, consider always the possible coexistence of an acquired immunodeficiency syndrome. PA can occasionally be an aggressive, disfigurating and disabling disease and the treatment (incisive and precocious) should be similar to that for rheumatoid arthritis. At present, a definitive therapy does not yet exist, but the majority of PA patients can lead a fairly normal life and they do not show increased mortality rates (excluding the severe cases of erythrodermic or pustulosis psoriasis). However, as a result of the various problems of occupation and morbidity it causes, PA is a disease with great social involvement.

摘要

本文旨在基于对近期文献的广泛批判性综述,探讨一名56岁男性患者的病例。该患者患有皮肤银屑病和残毁性银屑病关节炎(PA)(多关节、对称性、破坏性和侵蚀性),累及手、足和脊柱,伴有男性型肥胖和轻度2型糖尿病。患者的HLA分型显示为HLA - A3 - Ax、B14 - B63和Cw4 - Cw6单倍型,其中一些与PA易感性相关或有联系。皮肤银屑病是一种慢性炎症性皮肤病,可在任何年龄发病,影响约2%的西方人群。在5% - 7%的患者中,它与关节表现或真正的关节炎相关。PA是一种慢性、炎症性、血清阴性关节病,可能在一些银屑病患者中发生,可累及外周和中轴(脊柱关节炎)关节,并可能导致严重的关节破坏。遗传、免疫和环境(即感染因子或创伤)因素似乎在PA的发病和临床表现中起重要作用。虽然PA在临床上是一种单形性疾病,但它可能表现出不同的异质性亚组,其发病机制存在差异。当怀疑有PA时,必须仔细分析患者的家族史,认真寻找特定的皮肤特征,排除感染性关节炎(特别是如果累及单关节),并且在暴发性疾病的情况下,始终要考虑获得性免疫缺陷综合征的可能共存。PA偶尔可能是一种侵袭性、毁容性和致残性疾病,治疗(果断且早期)应与类风湿关节炎相似。目前,尚无明确的治疗方法,但大多数PA患者可以过上相当正常 的生活,并且他们没有显示出死亡率增加(不包括红皮病型或脓疱型银屑病的严重病例)。然而,由于它所导致的各种职业和发病问题,PA是一种具有重大社会影响的疾病。

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