Journal of the Japanese Society of Pediatric Surgeons
Online ISSN : 2187-4247
Print ISSN : 0288-609X
ISSN-L : 0288-609X
Clinical Aspects of Sarcomatous Renal Tumor of Childhood : I. A Report of Two Cases of Malignant Rhabdoid Tumor of Kidney(MRTK) With a Review of Japanese Literature
K. NakadaT. FujiokaY. KimM. IshikawaT. NoguchiM. TakagiUshigomeS.
Author information
JOURNAL FREE ACCESS

1987 Volume 23 Issue 1 Pages 114-121

Details
Abstract
This paper describes clinical characteristics of malignant rhabdoid tumor of the kidney(MATK) from our experiences and the literatures. In two infants experienced in our institute, the MRTK were found in association with brain tumors, one of which was cerebellar medulloblastoma and the other was metastatic MRTK. Both patients died of rapid growth of the brain tumors. For the last 15 years, only ten of infantile malignant renal tumors(MRTK or neonatal Wilms') had been reported in Japan. Among them, all of MRTK(five cases) had expired within one or eight months postoperatively. Associated brain tumors were found in three of five MRTK in this series. Since the rapid appearance of local recurrences or multiple metastases of the tumor is seen, additional extensive studis in attempt to develop the effective treatment for these highly malignant renal tumors are necessary.
Content from these authors
© 1987 The Japanese Society of Pediatric Surgeons

この記事はクリエイティブ・コモンズ [表示 - 非営利 - 継承 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-sa/4.0/deed.ja
Previous article Next article
feedback
Top