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Japanese

CONGENITAL RENAL ARTERIOVENOUS MALFORMATION:A CASE REPORT Masato Matsushita 1 , Atsuo Sugita 1 , Kensuke Ozu 1 , Tomohiko Okamura 1 , Senzi Hoshi 1 , Shunzo Kawamura 2 1Department of Urology, Tohoku University School of Medicine 2Department of Urology, Yamagata University School of Medicine pp.955-959
Published Date 1976/11/20
DOI https://doi.org/10.11477/mf.1413202255
  • Abstract
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A case of left congenital renal arteriovenous malformation in a 33 year-old woman with the chief complaint of sudden grosshematuria was reported.

Intravenous pyelography showed normal kidney and ureter, but retrograde pyeolgraphy disclosed irregurality of left ureteropelvic junction. Angiographic signs included small cirsoid vessels and early venous return, but there was no evidence of displacement of intrarenal vessels and collecting system. The size and weight of the left kidney were normal, but abnormal pelvic submucosal angiomatous vessels and phlebosclerotic changes of interlobar veins were histopathologically elicited.


Copyright © 1976, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1332 印刷版ISSN 0385-2393 医学書院

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