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Case Report
Journal of Korean Neurosurgical Society 1999;28(7): 1015-1022.
Malignant Rhabdoid Tumor.
Moon Kyu Kim, Moo Seong Kim, Sun Il Lee, Yong Tae Jung, Soo Chun Kim, Jae Hong Sim, Yeong Il Yang, Choong Ki Eun
1Department of Neurosurgery, College of Medicine, Inje University, Paik Hospital, Pusan.
2Department of Anatomic Pathology, College of Medicine, Inje University, Paik Hospital, Pusan.
3Department of Diagnostic Radiology, College of Medicine, Inje University, Paik Hospital, Pusan.
ABSTRACT
Primary CNS rhabdoid tumor is an extremely rare malignant tumor affecting children. Clinical, radiological, and histopathological features of malignant rhabdoid tumor are presented. Following the complete extirpation of a large tumor at the frontoparietal region, a 16-year-old male patient suffered from several local recurrences. The neoplasm is, defined by its histopathological and ultrastructural characteristics and by the pattern of its antigenicity as a malignant rhabdoid tumor(MRT).
Key Words: Malignant rhabdoid tumor; Recurrences; Ultrastructural
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