Handa S P, Tennant R
Postgrad Med J. 1968 Oct;44(516):792-8. doi: 10.1136/pgmj.44.516.792.
Two cases of medullary cystic disease of the kidney in two siblings are presented. In both siblings there was an insidious onset of azotaemia and anaemia at an early age. The urinalyses were normal except for a trace of proteinuria and persistent low specific gravity. The kidneys were small by radiological studies and this was proved at necropsy. The gross microscopic appearances of the kidneys were consistent with medullary cystic disease. The literature on this subject and current views on the similarities between familial juvenile nephronophthisis and this condition are discussed.
本文报告了一对 siblings 中两例肾髓质囊性疾病的病例。在这对 siblings 中,两人均在早年隐匿起病,出现氮质血症和贫血。除微量蛋白尿和持续低比重外,尿液分析均正常。影像学检查显示肾脏体积小,尸检证实了这一点。肾脏的大体和显微镜下表现与肾髓质囊性疾病相符。本文讨论了关于该主题的文献以及目前对家族性青少年肾单位肾痨与本病之间相似性的观点。