Paydaş S
Cukurova University, Faculty of Medicine, Department of Internal Medicine, Adana, Turkey.
Int Urol Nephrol. 2000;32(2):291-2. doi: 10.1023/a:1007196926394.
This report describes a patient with Familial Mediterranean Fever (FMF) associated with renal amyloidosis, bilaretal surrenal haematomas and hypoaldosteronism which was clinically asymptomatic. The deposition of AA amyloide was found on the renal and bone marrow biopsies. Bilateral surrenal haematoma regressed after six month from the first events. Colchicine therapy controlled the attacks of the disease.
本报告描述了一名患有家族性地中海热（FMF）的患者，该患者伴有肾淀粉样变性、双侧肾上腺血肿和临床无症状的醛固酮减少症。在肾活检和骨髓活检中发现了AA淀粉样蛋白沉积。双侧肾上腺血肿在首次发病后六个月消退。秋水仙碱治疗控制了疾病的发作。
