作者: Sandra H. Preissig , Michael T. Smith , Howard W. Huntington
DOI: 10.1002/1097-0142(197907)44:1<281::AID-CNCR2820440148>3.0.CO;2-B
关键词: Medicine 、 Pinealoma 、 Teratoma 、 Pathology 、 Radiation therapy 、 Rhabdomyosarcoma 、 Pineal Teratoma 、 Cancer research 、 Oncology
摘要: Pineal teratomas are relatively uncommon intracranial neoplasms. A rhabdomyosarcoma developed in a pineal teratoma 14-year-old boy and was rapidly fatal despite radiation therapy. This is the second reported case of giving rise to rhabdomyosarcoma.