TY - JOUR
T1 - Atypical teratoid/rhabdoid tumor
T2 - Analysis of cytomorphologic features in CSF, focused on the differential diagnosis from mimickers
AU - Choi, Junjeong
AU - Kim, Hoguen
AU - Kim, Se Hoon
PY - 2012/7
Y1 - 2012/7
N2 - Atypical teratoid and rhabdoid tumor (AT/RT) is a rare tumor with fatal clinical consequences, usually affecting young children. A significant portion of patients present with dissemination to cerebrobspinal fluid (CSF). However, a limited number of studies are available regarding the cytomorphologic findings of AT/RT in CSF. We collected eight cases of CSF cytology of AT/RT and describe the cytomorphologic features of AT/RT in CSF. Typical rhabdoid cells are found in most cases and they are characterized by eccentric nuclei, abundant cytoplasm, and clustering of the tumor cells. The presence of these cells in CSF indicates disseminated diseases and aggressive therapeutic consideration for patient management is required.
AB - Atypical teratoid and rhabdoid tumor (AT/RT) is a rare tumor with fatal clinical consequences, usually affecting young children. A significant portion of patients present with dissemination to cerebrobspinal fluid (CSF). However, a limited number of studies are available regarding the cytomorphologic findings of AT/RT in CSF. We collected eight cases of CSF cytology of AT/RT and describe the cytomorphologic features of AT/RT in CSF. Typical rhabdoid cells are found in most cases and they are characterized by eccentric nuclei, abundant cytoplasm, and clustering of the tumor cells. The presence of these cells in CSF indicates disseminated diseases and aggressive therapeutic consideration for patient management is required.
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U2 - 10.1002/dc.21594
DO - 10.1002/dc.21594
M3 - Article
C2 - 21197644
AN - SCOPUS:84862522383
SN - 8755-1039
VL - 40
SP - 592
EP - 596
JO - Diagnostic Cytopathology
JF - Diagnostic Cytopathology
IS - 7
ER -