Cystic Glioblastoma Rupturing into the Ventricle.

cyst glioblastoma rupture ventricle

Journal

NMC case report journal
ISSN: 2188-4226
Titre abrégé: NMC Case Rep J
Pays: Japan
ID NLM: 101692589

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 03 03 2019
accepted: 10 07 2019
entrez: 16 1 2020
pubmed: 16 1 2020
medline: 16 1 2020
Statut: epublish

Résumé

Cystic tumors, such as craniopharyngiomas and Rathke's cleft cysts, as well as arachnoid cysts have been reported to rupture occasionally. Approximately 8-10% of glioblastomas (GBMs) are known to have a significant cystic component; however, to the best of our knowledge, no studies have reported cystic rupturing of GBMs. Here, we describe a unique case of cystic GBM rupturing and penetrating into the cerebral ventricle. A 77-year-old man with a right frontal lobe lesion suspected as GBM with a large cyst was referred to our hospital. At admission, disorientation and left facial weakness were detected. Consciousness disturbance worsened on the 8th day of hospitalization. Computed tomography (CT) revealed prominent shrinkage of the tumor and intratumoral cyst. Signs of meningeal irritation were observed, and chemical meningitis due to cystic tumor rupture and leakage of necrotic components into the ventricle was highly suspected. Surgical resection of the right frontal lobe tumor was performed on the 10th day of hospitalization. During the surgery, clear and colorless cerebrospinal fluid was obtained upon penetration of the tumoral cyst, suggesting traffic of tumor cysts and cerebral ventricle. Adjuvant chemoradiation therapy was initiated postoperatively. Local recurrence was noted at the corpus callosum 7 months postoperatively and was treated with a gamma knife. Further therapy was performed after this recurrence. However, his condition gradually deteriorated 15 months postoperatively, and he was subjected to terminal care. To the best of our knowledge, this is the first report on a cystic GBM rupture.

Identifiants

pubmed: 31938681
doi: 10.2176/nmccrj.cr.2019-0043
pii: nmccrj-7-39
pmc: PMC6957778
doi:

Types de publication

Case Reports

Langues

eng

Pagination

39-41

Informations de copyright

© 2020 The Japan Neurosurgical Society.

Déclaration de conflit d'intérêts

Conflicts of Interest Disclosure There is no disclosure of funding as no financial support or grants supported this paper. No author has a personal or institutional financial interest in the drugs, materials, or devices described in this paper.

Références

Neurol Med Chir (Tokyo). 2010;50(3):254-6
pubmed: 20339281
Med Hypotheses. 2006;66(4):801-4
pubmed: 16321475
J Neurosurg. 2004 Jan;100(1):61-7
pubmed: 14743913
Neurol Med Chir (Tokyo). 2003 Mar;43(3):150-2
pubmed: 12699125
J Neurosurg. 2013 Apr;118(4):786-98
pubmed: 23176331
J Neurosurg. 1980 Dec;53(6):821-5
pubmed: 6255113

Auteurs

Yoshimichi Sato (Y)

Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Ryuta Saito (R)

Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Masayuki Kanamori (M)

Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Teiji Tominaga (T)

Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Classifications MeSH