Malignant rhabdoid tumor: Difference between revisions

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{{SK}} Malignant rhabdoid tumor; Malignant rhabdoid neoplasm; Atypical teratoid rhabdoid tumor


==Overview==
==Overview==

Revision as of 16:14, 22 December 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]

Synonyms and keywords: Malignant rhabdoid tumor; Malignant rhabdoid neoplasm; Atypical teratoid rhabdoid tumor

Overview

  • Malignant rhabdoid tumor is one of the aggressive tumors in the pediatric population. It was originally described as a rhabdomyosarcomatoid variant of Wilms' tumor, which is primarily a kidney tumor.[1]
  • Malignant rhabdoid tumor was first described as a variant of Wilms' tumor of the kidney, in 1978.
  • Common locations associated with malignant rhabdoid tumor include:[2]
  • Almost all reported cases of malignant rhabdoid tumor, regardless of site of origin, occur in young children between birth and 2 years of age.[3]
  • In approximately 10% of cases of renal malignant rhabdoid tumor, the patients subsequently develop intracranial atypical teratoid rhabdoid tumor.

References

  1. Malignant rhabdoid tumour. Wikipedia 2015. https://en.wikipedia.org/wiki/Malignant_rhabdoid_tumour. Accessed on December 22, 2015
  2. Rhabdoid tumours. Dr Ayush Goel and A.Prof Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/rhabdoid-tumours. Accessed on December 22, 2015
  3. Epidemiology of rhabdoid tumours. Dr Ayush Goel and A.Prof Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/rhabdoid-tumours. Accessed on December 22, 2015

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