Asklepios Klinik Altona, Rheumatologie, Klinische Immunologie Nephrologie, Paul-Ehrlich-Strasse 1, 22763, Hamburg, Germany.
Medizinische Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Charité Mitte, Charitéplatz 1, 10117, Berlin, Germany.
Rheumatol Int. 2019 Nov;39(11):2005-2014. doi: 10.1007/s00296-019-04410-9. Epub 2019 Aug 10.
Idiopathic antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are a group of diseases that are often difficult to diagnose due to the wide range of clinical manifestations. Notably, renal involvement is a serious organ complication, which usually requires intensive immunosuppressive therapy and is prone to recurrence. In recent years, there has been some progress regarding the understanding of the pathogenesis of the diseases. It has been shown that both cocaine and levamisole, which is a common adulterant of cocaine, can trigger the formation of ANCAs and lead to the corresponding symptoms. We report two cases of AAV with different renal manifestations associated with cocaine consumption. Furthermore, we performed a review of the literature to identify, characterize and describe histologically documented cases of renal involvement in AAV, related to cocaine abuse. Cocaine/levamisole-induced vasculitis may, therefore, mimic idiopathic AAV. Although the detection of ANCA and anti-PR3 (proteinase 3, PR3) as well as anti-MPO antibodies (myeloperoxidase, MPO) are the serological hallmark of idiopathic AAV, certain clinical- and antibody constellations should lead to consideration of illicit drugs as inductors of the disease. Especially in young patients, certain serologic constellations (e.g., PR3 and MPO double positivity, positive antinuclear antibodies, low complement level, and positive testing for antiphospholipid antibodies), skin involvement, musculoskeletal symptoms and hematologic (anemia, leukopenia) affections should prompt testing for cocaine and levamisole consumption via urine drug testing. Treatment includes both immunosuppressive approaches and drug cessation but is difficult since many patients continue cocaine consumption.
特发性抗中性粒细胞胞浆抗体 (ANCA) 相关性血管炎 (AAV) 是一组疾病,由于临床表现广泛,通常难以诊断。值得注意的是,肾脏受累是一种严重的器官并发症,通常需要强化免疫抑制治疗且容易复发。近年来,人们对疾病的发病机制有了一些了解。已经表明,可卡因和作为可卡因常见掺杂物的左旋咪唑都可以触发 ANCAs 的形成,并导致相应的症状。我们报告了两例与可卡因消费相关的不同肾脏表现的 AAV 病例。此外,我们对文献进行了回顾,以确定、描述和描述与可卡因滥用相关的 AAV 中肾脏受累的组织学记录病例。可卡因/左旋咪唑诱导的血管炎可能模仿特发性 AAV。虽然 ANCA 和抗 PR3(蛋白酶 3,PR3)以及抗 MPO 抗体(髓过氧化物酶,MPO)的检测是特发性 AAV 的血清学标志,但某些临床和抗体组合应考虑将非法药物作为疾病的诱导物。特别是在年轻患者中,某些血清学组合(例如,PR3 和 MPO 双重阳性、抗核抗体阳性、补体水平低、抗磷脂抗体阳性)、皮肤受累、肌肉骨骼症状和血液学(贫血、白细胞减少)影响应提示通过尿液药物检测检测可卡因和左旋咪唑的使用。治疗包括免疫抑制方法和药物停用,但由于许多患者继续使用可卡因,因此治疗较为困难。