Chordoma of the corpus callosum: case report.

brain neoplasms chordoma corpus callosum oncology

Journal

Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357

Informations de publication

Date de publication:
01 11 2019
Historique:
received: 15 04 2018
accepted: 11 06 2018
medline: 1 12 2018
pubmed: 1 12 2018
entrez: 1 12 2018
Statut: epublish

Résumé

Chordomas are neoplasms that typically arise from midline skeletal structures and rarely originate within the intradural compartment of the CNS. A chordoma arising from the corpus callosum has not been previously described. The authors report the surgical management of a chordoma originating within the splenium of the corpus callosum. To determine the incidence and distribution of intracranial intradural chordoma, a literature search for additional cases was performed. MEDLINE was searched using the MeSH keyword "chordoma," yielding 2010 articles. These articles were screened for cases of primary intradural chordoma rostral to the craniocervical junction, which led to the identification of 46 relevant articles. The authors report the case of a 69-year-old man who initially presented with nonspecific neurological symptoms including spatial disorientation and cognitive decline. These symptoms eventually prompted intracranial imaging, including MRI, which revealed a ring-enhancing, heterogeneous, cystic mass localized within the splenium of the corpus callosum and extending into the bilateral ventricles. The lesion was believed to represent a high-grade glioma and the patient underwent a left interhemispheric approach and subtotal resection. After pathologic evaluation confirmed a diagnosis of an anaplastic chordoma, the patient underwent further resection. A gross-total resection (GTR) was achieved with a transfalcine approach to the contralateral portion of the tumor. Postoperatively, the patient had a partial left homonymous quadrantanopsia, but was otherwise at his neurological baseline. Proton beam radiotherapy was performed to the resection cavity but diffuse intraventricular disease ensued. The results of a literature search suggest that a chordoma arising in the corpus callosum has not been previously described. The present case demonstrates that chordomas can occur in the corpus callosum, and illustrates the utility of a transfalcine approach for GTR of lesions in this location, as well as the need for improved strategies to prevent intraventricular dissemination.

Identifiants

pubmed: 30497142
doi: 10.3171/2018.6.JNS181028
pii: 2018.6.JNS181028
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

1380-1386

Auteurs

Lorenzo Rinaldo (L)

Departments of1Neurosurgery.

David S Priemer (DS)

2Department of Anatomic Pathology and Neuropathology, Indiana University School of Medicine, Indianapolis, Indiana.

Alexander O Vortmeyer (AO)

2Department of Anatomic Pathology and Neuropathology, Indiana University School of Medicine, Indianapolis, Indiana.

Aaron A Cohen-Gadol (AA)

3Goodman Campbell Brain and Spine, Indiana University Department of Neurological Surgery, Indianapolis, Indiana; and.

Daniel J Brat (DJ)

4Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Anita Mahajan (A)

5Radiation Oncology, and.

Caterina Giannini (C)

Departments of1Neurosurgery.
6Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

Terry C Burns (TC)

Departments of1Neurosurgery.

Classifications MeSH