Stave G M, Croker B P
Arch Pathol Lab Med. 1984 Sep;108(9):747-51.
A review was made of the clinical histories, treatment, and renal histologic features of 12 patients with anti-glomerular basement membrane antibody-induced glomerulonephritis (anti-GBM disease). Two patients had milder histopathologic changes in their kidney biopsy specimens and achieved clinical remission. The other ten patients with severe lesions in their biopsy specimens progressed to renal failure. In addition, vascular lesions of thrombotic microangiopathy were present in six of 12 patients. Six patients had clinical laboratory evidence of microangiopathic hemolytic anemia. There are two important points to be noted from this study. First, the kidney biopsy specimen may be a useful indicator of disease severity and prognosis. Second, clinical laboratory or histologic evidence of thrombotic microangiopathy may occur in 75% of patients with anti-GBM disease.
对12例抗肾小球基底膜抗体诱导的肾小球肾炎(抗GBM病)患者的临床病史、治疗及肾脏组织学特征进行了回顾。2例患者肾脏活检标本的组织病理学改变较轻并实现了临床缓解。另外10例活检标本有严重病变的患者进展为肾衰竭。此外,12例患者中有6例存在血栓性微血管病的血管病变。6例患者有微血管病性溶血性贫血的临床实验室证据。从这项研究中有两点需要注意。第一,肾脏活检标本可能是疾病严重程度和预后的有用指标。第二,75%的抗GBM病患者可能出现血栓性微血管病的临床实验室或组织学证据。