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肺肾综合征

Pulmonary-renal syndromes.

作者信息

Brusselle G G

机构信息

Department of Respiratory Diseases, University Hospital Ghent, De Pintelaan 185, B-9000 Gent, Belgium.

出版信息

Acta Clin Belg. 2007 Mar-Apr;62(2):88-96. doi: 10.1179/acb.2007.016.

Abstract

Pulmonary-renal syndromes or lung-kidney syndromes are clinical syndromes defined by a combination of diffuse alveolar haemorrhage (DAH) and glomerulonephritis. Pulmonary-renal syndromes are not a single entity, but are caused by a wide variety of diseases, including various forms of primary systemic vasculitis (especially Wegener's granulomatosis and microscopic polyangiitis), Goodpasture's syndrome (associated with autoantibodies to the alveolar and glomerular basement membrane) and systemic lupus erythematosus. The diagnosis rests on the identification of particular patterns of clinical, radiologic, pathologic and laboratory features. Serologic testing is important in the diagnostic work-up of patients presenting with a pulmonary-renal syndrome. The majority of cases of pulmonary-renal syndrome are associated with ANCAs, either c-ANCA or p-ANCA, due to autoantibodies against the target antigens proteinase-3 and myeloperoxidase respectively. The antigen target in Goodpasture's syndrome is type IV collagen, the major component of basement membranes. Diffuse alveolar haemorrhage is characterized by the presence of a haemorrhagic bronchoalveolar lavage (BAL) in serial BAL samples. In the clinical setting of an acute nephritis syndrome, percutaneous renal biopsy is commonly performed for histopathology and immunofluorescence studies. Treatment of generalized ANCA-associated vasculitis consists of corticosteroids and immunosuppressive agents such as cyclophosphamide (as induction therapy) or azathioprine (as maintenance therapy once remission has been achieved). The combination of plasmapheresis with these cytotoxic agents and steroids is effective in patients with Goodpasture's syndrome, especially if instituted early in the course of the disease. Recent evidence suggests that patients with severe ANCA-associated vasculitis, defined by the presence of diffuse alveolar haemorrhage and/or severe renal involvement (creatinine concentration > 5.7 mg/dl), might benefit from plasma exchange in combination with cyclophosphamide and corticosteroids.

摘要

肺肾综合征是由弥漫性肺泡出血(DAH)和肾小球肾炎共同构成的临床综合征。肺肾综合征并非单一疾病实体,而是由多种疾病引起,包括各种原发性系统性血管炎(尤其是韦格纳肉芽肿和显微镜下多血管炎)、古德帕斯彻综合征(与抗肺泡和肾小球基底膜自身抗体相关)以及系统性红斑狼疮。诊断依赖于对特定临床、放射学、病理学和实验室特征模式的识别。血清学检测在肺肾综合征患者的诊断检查中很重要。肺肾综合征的大多数病例与抗中性粒细胞胞浆抗体(ANCA)相关,即分别针对靶抗原蛋白酶-3和髓过氧化物酶的c-ANCA或p-ANCA。古德帕斯彻综合征的抗原靶点是IV型胶原,它是基底膜的主要成分。弥漫性肺泡出血的特征是在连续的支气管肺泡灌洗(BAL)样本中出现血性灌洗液。在急性肾炎综合征的临床情况下,通常进行经皮肾活检以进行组织病理学和免疫荧光研究。全身性ANCA相关血管炎的治疗包括使用皮质类固醇和免疫抑制剂,如环磷酰胺(作为诱导治疗)或硫唑嘌呤(在病情缓解后作为维持治疗)。血浆置换与这些细胞毒性药物和类固醇联合使用对古德帕斯彻综合征患者有效,尤其是在疾病早期开始治疗时。最近的证据表明,由弥漫性肺泡出血和/或严重肾脏受累(肌酐浓度>5.7mg/dl)定义的严重ANCA相关血管炎患者,可能从血浆置换联合环磷酰胺和皮质类固醇治疗中获益。

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