可卡因/左旋咪唑诱导的皮肤局限性anca相关血管炎伴坏疽样脓皮病。

IF 1.7 Q3 DERMATOLOGY
Mirjana Urosevic-Maiwald, Jan-Hendrik B Hardenberg, Jürg Hafner, Marie-Charlotte Brüggen
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引用次数: 0

摘要

左旋咪唑作为可卡因最常见的掺假剂的使用已经合并了以前未知的毒性,特别是一种称为可卡因/左旋咪唑相关自身免疫综合征(CLAAS)的疾病实体。临床上,CLAAS可表现为多种皮肤和皮外特征,具有共同的实验室表现(中性粒细胞减少,自身抗体模式)。我们报告的情况下,可卡因滥用的女性患者复发发作疼痛的溃疡,恶化和扩大超过三年的时间。该病例表现出药物诱导、皮肤受限、anca相关血管炎的所有特征,随着时间的推移演变为pg样表现。在这两个疾病阶段,患者对停止可卡因暴露和全身糖皮质激素反应良好。本病例在单个患者中显示了皮肤CLAAS表现的连续性。CLAAS已成为高危可卡因使用者群体中的一个主要公共卫生问题,临床医生在治疗出现单一或多重皮肤溃疡的可卡因使用者时应警惕这种情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cocaine/Levamisole-Induced, Skin-Limited ANCA-Associated Vasculitis with Pyoderma Gangrenosum-like Presentation.

Cocaine/Levamisole-Induced, Skin-Limited ANCA-Associated Vasculitis with Pyoderma Gangrenosum-like Presentation.

The use of levamisole as the most frequent adulterant of cocaine has merged in previously unknown toxicities, notably a disease entity called cocaine/levamisole-associated autoimmune syndrome (CLAAS). Clinically, CLAAS can manifest with diverse cutaneous and extracutaneous features sharing common laboratory findings (neutropenia, autoantibody patterns). We report the case of a cocaine-abusing female patient with relapsing episodes of painful ulcers, worsening and expanding over a three-year period. The case exhibited all features of a drug-induced, skin-limited, ANCA-associated vasculitis, evolving over time to PG-like findings. In both disease stages, the patient responded well to the cessation of cocaine exposure and systemic glucocorticosteroids. This case demonstrates the continuous nature of cutaneous CLAAS manifestations in a single patient. CLAAS has become a major public health issue in the at-risk group of cocaine users, and clinicians should be alert of this condition when treating cocaine users presenting with single or multiple skin ulcerations.

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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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