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Voisin, M. R., Ovenden, C., Tsang, D. S., Gupta, A. A., Huang, A., Gao, A. F. et al. (2019). Atypical Teratoid/Rhabdoid Sellar Tumor in an Adult with a Familial History of a Germline SMARCB1 Mutation: Case Report and Review of the Literature. World Neurosurgery, 127, 336-345.
https://doi.org/10.1016/j.wneu.2019.04.083

has been cited by the following article:

• TITLE: Proposal of a New Therapeutic Approach for Adult Atypical Teratoid/Rhabdoid Tumor Based on Literature Review and Case Report

  AUTHORS: Nathan Gaquere, Maxime Rivollier, Philippe Colin, Claude-Fabien Litré, Jean-Charles Kleiber

  KEYWORDS: Adult, Atypical Teratoid/Rhabdoid Tumor, Brain, Childhood Tumor, Survival

  JOURNAL NAME: Voice of the Publisher, Vol.11 No.1, March 24, 2025

  ABSTRACT: Rhabdoid tumors are aggressive soft tissue sarcomas predominantly affecting children under three years of age. While rare, cases of Atypical Teratoid/Rhabdoid Tumors (AT/RT) have been reported in adults, presenting unique challenges for treatment. This article presents a new therapeutic approach for adult AT/RT based on a case report and literature review. The case involves an adult male diagnosed with AT/RT who achieved a ten-year survival through a comprehensive treatment regimen. The approach includes surgical resection, intensive chemotherapy, and radiation therapy. The study highlights the importance of adopting an intensive chemotherapy protocol, typically used in pediatric cases, as a promising strategy for adult AT/RT management. This innovative proposal underscores the need for further research and therapeutic advancements to improve outcomes in this rare disease.