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緒言
いわゆる特発性後腹膜線維化症は,1905年にAlbarren1)が初めて報告して以来現在までに外国における報告は数多くみられるようになつた。しかし,本邦における報告は著者らの蒐集した範囲では20数例のみである。最近われわれは典型的な特発性後腹膜線維化症と思われる1例を経験したのでこれを報告すると共に,本邦における特発性後腹膜線維化症について若干の統計的考察を加えてみたい。
A case of idiopathic retroperitoneal fibrosis in a 69 year old male with the chief complaint of uremic symptoms and oliguria, was reported. Both ureter were wrapped in a firm white fibrous mass with the middle portion at the bifurcation of abdominal aorta extending to the sacral promontory. End to end anastomosis of both ureter were performed after dissection and resection. The ureter was surro-unded by connective tissue with non-specific inflammation, histologically, but no remarkable changes were noticed in the muscle and cpithelium of mucous membrane.
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