J Korean Pediatr Soc.  1999 Sep;42(9):1292-1297.

A Case of Malignant Extrarenal Rhabdoid Tumor

Affiliations
  • 1Department of Pediatrics, Wonju College of Medicine, Yonsei University, Wonju, Korea.
  • 2Department of Orthopedic Surgery, Wonju College of Medicine, Yonsei University, Wonju, Korea.
  • 3Department of Pathology, Wonju College of Medicine, Yonsei University, Wonju, Korea.
  • 4Department of Radiology, Wonju College of Medicine, Yonsei University, Wonju, Korea.

Abstract

Malignant Rhabdoid tumor is a rare malignant neoplasm and is morphologically similar to rhabdomyosarcoma, but is different immunohistochemically. Most malignant rhabdoid tumors occur in the kidney of infants, and are rarely reported at extrarenal sites. Since Frierson and his collagues first described the malignant extrarenal rhabdoid tumor(MRT) in children in 1985, it has rarely been reported. The neoplasm is histologically and immunohistochemically identical to a renal malignant rhabdoid tumor. There have been no previous reports of this neoplasm in Korea. An MRT of the sacroiliac bone in a 11-year-old girl is described. Five months after the initial presentation, the patient is still alive with partial response to combination chemotherapy and radiotherapy. The authors review previous reports of extrarenal MRT, and discuss the pathologic characteristics, differential diagnosis, and treatment of this rare neoplasm.

Keyword

Malignant rhabdoid tumor; Extrarenal

MeSH Terms

Child
Diagnosis, Differential
Drug Therapy, Combination
Female
Humans
Infant
Kidney
Korea
Radiotherapy
Rhabdoid Tumor*
Rhabdomyosarcoma
Full Text Links
  • KJP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr