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WILMS' TUMOR IN A CHILD WITH CONGENITAL ANIRIDIA Yoshiharu Hiratsuka 1 , Kimitaka Sakamoto 1 , Kazuko Tahara 2 , Kenji Ohshima 2 1Departments of Urology , School of Medicine Fukuoka University 2Departments of Ophthalmology , School of Medicine Fukuoka University pp.271-274
Published Date 1978/3/20
DOI https://doi.org/10.11477/mf.1413202521
  • Abstract
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A boy, who had a congenital aniridia and an undescended testis, had several pyelographies since 8-month old because of the increasing risk that Wilms' tumor could develop. When he was 2-year 2-month old, IVY and renal arteriography showed a space-occupying lesion diagnosed as a left Wilms' tumor.

The tumor was completely removed by radical nephrectomy. Actinomycin D has been administered internittently after surgery. The child is now 3-year 5-month old and healthy without any evidence of metastasis, recurrence or contralateral occurrence.


Copyright © 1978, 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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