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Intraventricular Glioblastomas.

Identifieur interne : 000311 ( Main/Exploration ); précédent : 000310; suivant : 000312

Intraventricular Glioblastomas.

Auteurs : Atef Ben Nsir [Tunisie] ; Yassine Gdoura [Tunisie] ; Quoc-Anh Thai [États-Unis] ; Alia Zhani Kassar [Tunisie] ; Nejib Hattab [Tunisie] ; Hafedh Jemel [Tunisie]

Source :

RBID : pubmed:26773981

Descripteurs français

English descriptors

Abstract

BACKGROUND AND IMPORTANCE

Although glioblastoma is the most common primary brain tumor, primary intraventricular locations are extremely rare; only 21 cases have been reported to date.

METHODS

A retrospectively acquired database of all intracranial glioblastomas treated in 2 different neurosurgical departments during the last 10 years was queried. Patients with histologically proven intraventricular glioblastomas were included in the study.

RESULTS

Eight patients were identified as having a histologically confirmed intraventricular glioblastoma. Patient age at diagnosis ranged from 6 to 74 years (mean 29.6 years) and the male/female ratio was 5:3. Increased intracranial pressure due to hydrocephalus was the main cause of the clinical manifestations. The tumor was located within the lateral ventricle in 6 cases and the anterior third ventricle in 2 others. Gross total tumor excision was achieved in 3 patients, whereas the surgical resection was subtotal in 4 cases and a surgical biopsy was performed in 1 patient. Postoperative adjuvant therapies were administered in 5 patients. Median survival time was 32.1 months, and 3 patients were alive at the end of study. All of them had isocitrate dehydrogenase-mutated tumors.

CONCLUSIONS

Intraventricular glioblastoma is extremely rare and can affect younger individuals including children. This malignant tumor should be included in the differential diagnosis of intraventricular lesions, especially in the lateral ventricles. Radical surgical resection can be associated with remarkable disease-free survival, especially in isocitrate dehydrogenase-mutated tumors. Because recurrence virtually is unavoidable, long-term follow-up is mandatory.


DOI: 10.1016/j.wneu.2015.12.079
PubMed: 26773981


Affiliations:


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<term>Adolescent (MeSH)</term>
<term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Cerebral Ventricle Neoplasms (pathology)</term>
<term>Cerebral Ventricle Neoplasms (surgery)</term>
<term>Child (MeSH)</term>
<term>Diagnosis, Differential (MeSH)</term>
<term>Female (MeSH)</term>
<term>Glioblastoma (pathology)</term>
<term>Glioblastoma (surgery)</term>
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<term>Neurosurgical Procedures (methods)</term>
<term>Rare Diseases (pathology)</term>
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<term>Adolescent (MeSH)</term>
<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Diagnostic différentiel (MeSH)</term>
<term>Enfant (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Glioblastome (anatomopathologie)</term>
<term>Glioblastome (chirurgie)</term>
<term>Humains (MeSH)</term>
<term>Jeune adulte (MeSH)</term>
<term>Maladies rares (anatomopathologie)</term>
<term>Maladies rares (chirurgie)</term>
<term>Mâle (MeSH)</term>
<term>Procédures de neurochirurgie (méthodes)</term>
<term>Résultat thérapeutique (MeSH)</term>
<term>Sujet âgé (MeSH)</term>
<term>Tumeurs des ventricules cérébraux (anatomopathologie)</term>
<term>Tumeurs des ventricules cérébraux (chirurgie)</term>
<term>Études longitudinales (MeSH)</term>
<term>Études rétrospectives (MeSH)</term>
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<term>Glioblastome</term>
<term>Maladies rares</term>
<term>Tumeurs des ventricules cérébraux</term>
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<term>Glioblastome</term>
<term>Maladies rares</term>
<term>Tumeurs des ventricules cérébraux</term>
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<term>Neurosurgical Procedures</term>
</keywords>
<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr">
<term>Procédures de neurochirurgie</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Cerebral Ventricle Neoplasms</term>
<term>Glioblastoma</term>
<term>Rare Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en">
<term>Cerebral Ventricle Neoplasms</term>
<term>Glioblastoma</term>
<term>Rare Diseases</term>
</keywords>
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<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Child</term>
<term>Diagnosis, Differential</term>
<term>Female</term>
<term>Humans</term>
<term>Longitudinal Studies</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Retrospective Studies</term>
<term>Treatment Outcome</term>
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<term>Adulte</term>
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<term>Enfant</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Mâle</term>
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<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND AND IMPORTANCE</b>
</p>
<p>Although glioblastoma is the most common primary brain tumor, primary intraventricular locations are extremely rare; only 21 cases have been reported to date.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>A retrospectively acquired database of all intracranial glioblastomas treated in 2 different neurosurgical departments during the last 10 years was queried. Patients with histologically proven intraventricular glioblastomas were included in the study.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Eight patients were identified as having a histologically confirmed intraventricular glioblastoma. Patient age at diagnosis ranged from 6 to 74 years (mean 29.6 years) and the male/female ratio was 5:3. Increased intracranial pressure due to hydrocephalus was the main cause of the clinical manifestations. The tumor was located within the lateral ventricle in 6 cases and the anterior third ventricle in 2 others. Gross total tumor excision was achieved in 3 patients, whereas the surgical resection was subtotal in 4 cases and a surgical biopsy was performed in 1 patient. Postoperative adjuvant therapies were administered in 5 patients. Median survival time was 32.1 months, and 3 patients were alive at the end of study. All of them had isocitrate dehydrogenase-mutated tumors.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>Intraventricular glioblastoma is extremely rare and can affect younger individuals including children. This malignant tumor should be included in the differential diagnosis of intraventricular lesions, especially in the lateral ventricles. Radical surgical resection can be associated with remarkable disease-free survival, especially in isocitrate dehydrogenase-mutated tumors. Because recurrence virtually is unavoidable, long-term follow-up is mandatory.</p>
</div>
</front>
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