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可卡因-左旋咪唑诱导的皮肤血管炎和免疫介导性白细胞减少症综合征。

Syndrome of cocaine-levamisole-induced cutaneous vasculitis and immune-mediated leukopenia.

机构信息

Division of Rheumatology, Rhode Island Hospital and Warren Alpert School of Medicine at Brown University, Providence, RI 02905, USA.

出版信息

Semin Arthritis Rheum. 2011 Dec;41(3):434-44. doi: 10.1016/j.semarthrit.2011.05.009. Epub 2011 Aug 24.

Abstract

OBJECTIVE

We describe 4 patients who presented with palpable purpura, arthralgia or arthritis, leukopenia, and antineutrophil cytoplasmic antigen (ANCA) positivity most likely as a result of a hypersensitivity reaction to cocaine-levamisole induced vasculopathy.

METHODS

Cases were seen and reviewed in both the inpatient consult service and the outpatient clinics at Rhode Island Hospital from August 2009 to August 2010. Clinical characteristics as well as pertinent laboratory parameters were also reviewed and corroborated with a review of the present literature.

RESULTS

We describe 3 cases of cocaine-levamisole-related cutaneous vasculitis with or without associated neutropenia, and 1 case of severe neutropenia with oral mucosal ulceration. Further serologic studies revealed maximum titers of ANCA mostly in a perinuclear pattern. Antimyeloperoxidase tested negative or mildly elevated in our cohort. Three patients with neutropenia had positive antigranulocyte IgM antibody. Nonsteroidal anti-inflammatory drugs were effective as first-line treatment for joint pain. The use of colchicine and systemic corticosteroid was employed to manage severe and persistent skin lesions.

CONCLUSIONS

Cocaine-levamisole-related cutaneous vasculitis with leukopenia is a diagnosis of exclusion, but this diagnosis should be strongly considered in patients with a history of cocaine abuse who present with a tetrad of cutaneous manifestations consisting of palpable purpura or bullae with ear involvement, arthralgias, leukopenia, and positive ANCA in high titers and negative Antimyeloperoxidase, when other infectious or idiopathic vasculitic entities have been excluded.

摘要

目的

我们描述了 4 例患者,他们表现为可触及的紫癜、关节痛或关节炎、白细胞减少和抗中性粒细胞胞浆抗体(ANCA)阳性,最有可能是由于可卡因-左旋咪唑诱导的血管病变引起的过敏反应。

方法

2009 年 8 月至 2010 年 8 月,在罗德岛医院的住院咨询服务和门诊诊所中观察和回顾了这些病例。还回顾了临床特征以及相关的实验室参数,并结合现有文献进行了复习。

结果

我们描述了 3 例可卡因-左旋咪唑相关的皮肤血管炎,伴有或不伴有相关的中性粒细胞减少症,以及 1 例伴有严重中性粒细胞减少症和口腔黏膜溃疡的病例。进一步的血清学研究显示,ANCA 的最大滴度主要呈核周模式。在我们的队列中,抗髓过氧化物酶检测为阴性或轻度升高。3 例中性粒细胞减少症患者的抗粒细胞 IgM 抗体阳性。非甾体抗炎药是治疗关节痛的一线药物。秋水仙碱和全身皮质类固醇用于治疗严重和持续的皮肤病变。

结论

可卡因-左旋咪唑相关的皮肤血管炎伴白细胞减少是一种排除性诊断,但对于有可卡因滥用史且出现以下四种皮肤表现的患者,应强烈考虑该诊断:可触及的紫癜或大疱伴耳部受累、关节痛、白细胞减少和高滴度阳性的 ANCA 以及抗髓过氧化物酶阴性,当排除其他感染性或特发性血管炎实体时。

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