CSF cytology of atypical teratoid/rhabdoid tumor of the brain in a two-year-old girl: A case report

Citation
L. Lu et al., CSF cytology of atypical teratoid/rhabdoid tumor of the brain in a two-year-old girl: A case report, DIAGN CYTOP, 23(5), 2000, pp. 329-332
Citations number
14
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology
Journal title
DIAGNOSTIC CYTOPATHOLOGY
ISSN journal
87551039 → ACNP
Volume
23
Issue
5
Year of publication
2000
Pages
329 - 332
Database
ISI
SICI code
8755-1039(200011)23:5<329:CCOATT>2.0.ZU;2-Z
Abstract
Atypical teratoma/rhabdoid tumor (AT/RT) of the central nervous system is a highly malignant neoplasm in infants and early childhood. Approximately on e third of patients develop intracranial dissemination with involvement of cerebral spinal fluid(CSF). The clinical, radiological, and pathological fe atures have been described, bur cytology of the tumor cells in CSF has not. Multiple CSF samples were examined in a case of AT/RT in a 2-yr-old girl. The most consistent cytologic features of AT/RT are the large size of the t umor cells, eccentricity of the nuclei, and prominent nucleoli. The differe ntial diagnosis includes medulloblastoma/primitive neuroectodermal tumor (P NET) of the brain. Because AT/RT often contains PNET-like regions, the diff erential diagnosis mainly relies on the presence or absence of large rhabdo id tumor cells. Cytological examination of CSF from a patient with AT/RT is important in the early diagnosis, disease progression analysis and therapy modulation. Diagn. Cytopathol. 2000;23:329-332. (C) 2000 Wiley-Liss, Inc.