Saladi Lakshmi, Shaikh Danial, Saad Muhammad, Cancio-Rodriguez Enny, D'Agati Vivette D, Medvedovsky Boris, Uday Kalpana A, Adrish Muhammad
Division of Pulmonary and Critical Care Medicine Department of Medicine, Bronx Care Health System, Bronx, NY Department of Pathology, College of Physicians and Surgeons, Columbia University Affiliated with Icahn School of Medicine at Mount Sinai, New York, NY.
Medicine (Baltimore). 2018 Jun;97(23):e10954. doi: 10.1097/MD.0000000000010954.
Pulmonary renal syndrome (PRS) is a term most commonly used to describe a combination of glomerulonephritis and pulmonary hemorrhage as a manifestation of a multisystem autoimmune disease. It is usually associated with ANCA vasculitis and anti-GBM disease. Diffuse alveolar hemorrhage in a patient with ANCA and anti-GBM negative pauci-immune glomerulonephritis is rare and optimal management is unknown.
An 85-year-old man with hypertension, diabetes mellitus, prostate cancer and recently diagnosed pauci-immune necrotizing glomerulonephritis presented to our emergency department with worsening dyspnea and pedal edema for several days. Clinical presentation and radiological studies were suggestive of fluid overload but he developed worsening respiratory failure despite hemodialysis.
Bronchoscopy confirmed diffuse alveolar hemorrhage. ANCA and anti-GBM antibodies were negative. The patient was diagnosed with pulmonary renal syndrome - diffuse alveolar hemorrhage in the setting of ANCA and anti-GBM negative pauci-immune glomerulonephritis.
Patient was started on intravenous pulse steroids, cyclophosphamide and received seven sessions of plasmapheresis.
There was an improvement in patient's respiratory status and repeat bronchoscopy at the end of treatment did not show diffuse alveolar hemorrhage.
Pauci-immune crescentic necrotizing glomerulonephritis is usually associated with the presence of ANCA, however, ANCA may be absent in 10% of these cases. Immunosuppression is the mainstay of treatment for ANCA and anti-GBM associated PRS. This case highlights the importance of immunosuppression and plasmapheresis in patients with ANCA negative vasculitis due to presence of unidentified serum antibodies. If left untreated, these patients can have a fulminant course with high mortality ranging from 25 to 50%.
肺肾综合征(PRS)是一个最常用于描述肾小球肾炎和肺出血相结合的术语,它是多系统自身免疫性疾病的一种表现。它通常与抗中性粒细胞胞浆抗体(ANCA)血管炎和抗肾小球基底膜(GBM)疾病相关。在ANCA和抗GBM阴性的寡免疫性肾小球肾炎患者中出现弥漫性肺泡出血很罕见,最佳治疗方案尚不清楚。
一名85岁男性,患有高血压、糖尿病、前列腺癌,近期被诊断为寡免疫性坏死性肾小球肾炎,因呼吸困难加重和足部水肿数天前来我院急诊科就诊。临床表现和影像学检查提示液体超负荷,但尽管进行了血液透析,他的呼吸衰竭仍在加重。
支气管镜检查证实为弥漫性肺泡出血。ANCA和抗GBM抗体均为阴性。该患者被诊断为肺肾综合征——在ANCA和抗GBM阴性的寡免疫性肾小球肾炎背景下的弥漫性肺泡出血。
患者开始接受静脉注射脉冲类固醇、环磷酰胺治疗,并接受了七次血浆置换。
患者的呼吸状况有所改善,治疗结束时再次进行支气管镜检查未发现弥漫性肺泡出血。
寡免疫性新月体坏死性肾小球肾炎通常与ANCA的存在有关,然而,在10%的此类病例中可能不存在ANCA。免疫抑制是ANCA和抗GBM相关PRS的主要治疗方法。该病例强调了免疫抑制和血浆置换在ANCA阴性血管炎患者中的重要性,因为存在未识别的血清抗体。如果不进行治疗,这些患者可能会有暴发性病程,死亡率高达25%至50%。