TY - JOUR
T1 - Glioblastoma with Rhabdoid Features
T2 - Report of Two Young Adult Cases and Review of the Literature
AU - Miyahara, Makiko
AU - Nobusawa, Sumihito
AU - Inoue, Masato
AU - Okamoto, Kouichiro
AU - Mochizuki, Makoto
AU - Hara, Tetsuo
N1 - Publisher Copyright:
© 2016 Elsevier Inc. All rights reserved.
PY - 2016/2
Y1 - 2016/2
N2 - Background There are few previous reports of glioblastoma in young adults, in particular, of the very rare recently proposed rhabdoid or epithelioid types. Case Description We report 2 cases of glioblastoma with rhabdoid features involving a 27-year-old woman and a 41-year-old man. In case 1, the patient presented with generalized seizures, and the initial magnetic resonance imaging showed a very small region of contrast in the left parahippocampal area. After 1 year, the mass suddenly increased in size. Treatment with multiple therapies was administered, but 5 months later, the patient died from multiple systemic metastases. In case 2, the patient presented with a chief complaint of headache for a few weeks. Computed tomography and magnetic resonance imaging showed a left parietal mass with calcification and meningeal dissemination. After undergoing surgical removal, his condition rapidly deteriorated until brain death occurred. Conclusions Glioblastoma with rhabdoid features may represent a specific pattern of clinical progression that emerges from histologic glioblastoma types.
AB - Background There are few previous reports of glioblastoma in young adults, in particular, of the very rare recently proposed rhabdoid or epithelioid types. Case Description We report 2 cases of glioblastoma with rhabdoid features involving a 27-year-old woman and a 41-year-old man. In case 1, the patient presented with generalized seizures, and the initial magnetic resonance imaging showed a very small region of contrast in the left parahippocampal area. After 1 year, the mass suddenly increased in size. Treatment with multiple therapies was administered, but 5 months later, the patient died from multiple systemic metastases. In case 2, the patient presented with a chief complaint of headache for a few weeks. Computed tomography and magnetic resonance imaging showed a left parietal mass with calcification and meningeal dissemination. After undergoing surgical removal, his condition rapidly deteriorated until brain death occurred. Conclusions Glioblastoma with rhabdoid features may represent a specific pattern of clinical progression that emerges from histologic glioblastoma types.
KW - Composite extrarenal rhabdoid tumors
KW - Epithelioid glioblastoma
KW - Multiple systemic metastases
KW - Rhabdoid glioblastoma
UR - https://www.scopus.com/pages/publications/84975159373
U2 - 10.1016/j.wneu.2015.10.065
DO - 10.1016/j.wneu.2015.10.065
M3 - 記事
C2 - 26548829
AN - SCOPUS:84975159373
SN - 1878-8750
VL - 86
SP - 515.e1-515.e9
JO - World Neurosurgery
JF - World Neurosurgery
ER -