J Korean Neurosurg Soc.  2005 Nov;38(5):387-389.

Atypical Teratoid Rhabdoid Tumors in Adult Patient with Multiple Lesions

Affiliations
  • 1Department of Neurosurgery, Research Institute of Clinical Medicine, Chonbuk National University Medical School and Hospital, Jeonju, Korea. hayoungc@chonbuk.ac.kr

Abstract

Primary atypical teratoid/rhabdoid tumor(AT/RT) of the central nervous system is a recently described, highly malignant neoplasm that usually occur in the posterior fossa of children. Although AT/RT usually occurs in young children, AT/RT is being recognized in adults with increasing frequency. The authors report 49-year-old man with multiple AT/RT lesions (right lateral ventricle, right temporal lobe and right cerebellum). Histopathologic findings showed typical rhabdoid cells with eccentric nuclei and prominent nucleoli. Eventhough the tumor was removed, a patient was dead in one month after surgery due to recurrence and rapid regrowth of the tumor.

Keyword

AT/RT (Atypical teratoid rhabdoid tumor); Adult

MeSH Terms

Adult*
Central Nervous System
Child
Humans
Lateral Ventricles
Middle Aged
Recurrence
Rhabdoid Tumor*
Temporal Lobe
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