Berge E, Os I, Skjørten F, Svalander C
Akuttmedisinsk avdeling, Ullevål sykehus, Oslo.
Tidsskr Nor Laegeforen. 1995 Mar 10;115(7):823-6.
The association between deficiency of alpha-1-antitrypsin (A1AT) and glomerulonephritis has been only sporadically reported on, as opposed to the linkage between A1AT-deficiency and lung emphysema or hepatic cirrhosis. We describe the case of a 30-year-old man with A1AT deficiency who developed hepatic cirrhosis in early childhood, and IgA glomerulonephritis and hypertension in adult life. The IgA nephritis followed an unusual course. After three years of slight elevation of serum creatinine levels, the patient rapidly developed renal failure necessitating acute hemodialysis. The deterioration of the renal function was preceded by eruption of skin lesions, believed to represent a vasculitis. After six months of hemodialysis, the patient successfully received a transplanted kidney from his mother. The literature is reviewed with respect to the association between A1AT-deficiency and renal disease. We discuss possible underlying causes for the rapid deterioration of renal function in this patient.
与α-1抗胰蛋白酶(A1AT)缺乏和肺气肿或肝硬化之间的联系不同,α-1抗胰蛋白酶(A1AT)缺乏与肾小球肾炎之间的关联仅偶有报道。我们描述了一名30岁A1AT缺乏男性的病例,该患者在幼儿期患肝硬化,成年后患IgA肾小球肾炎和高血压。该IgA肾病病程异常。血清肌酐水平轻微升高三年后,患者迅速发展为肾衰竭,需要进行急性血液透析。肾功能恶化之前出现了皮肤病变,据信这代表血管炎。血液透析六个月后,患者成功接受了来自其母亲的移植肾。本文就A1AT缺乏与肾脏疾病之间的关联进行了文献综述。我们讨论了该患者肾功能迅速恶化的可能潜在原因。