INTRAVENTRICULAR DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR

Author:

Altinörs Nur1,Calisaneller Tarkan1,Gülşen Salih1,Özen Özlem2,Öngürü Önder3

Affiliation:

1. Department of Neurosurgery, Baskent University School of Medicine, Ankara, Turkey

2. Department of Pathology, Baskent University School of Medicine, Ankara, Turkey

3. Department of Pathology, Gulhane Military Medicine Academy, Ankara, Turkey

Abstract

Abstract OBJECTIVE The most common localization of dysembryoplastic neuroepithelial tumors (DNTs) is the supratentorial cortex, often in the temporal lobe. However, intraventricular localization of a DNT is extremely rare. CLINICAL PRESENTATION A 30-year-old woman presented with a 1-year history of epileptic seizures. The seizures had not been controlled despite standard doses of antiepileptics. INTERVENTION Neuroimaging results demonstrated a lesion located in the occipital horn of the right lateral ventricle. The lesion was totally removed. Based on histopathological and immunohistochemical evaluation, a DNT was diagnosed. Over the course of the next 8 months, the patient's epileptic seizures were under control. The most recent neuroimaging examinations revealed neither residual nor recurrent tumor. CONCLUSION Because DNTs are surgically curable and neither radiotherapy nor chemotherapy is required after surgery, recognition of an intraventricular DNT in this location is extremely important.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Surgery

Reference18 articles.

1. Dysembryoplastic neuroepithelial tumor-like neoplasm of the septum pellucidum: A lesion often misdiagnosed as glioma: Report of 10 cases;Baisden;Am J Surg Pathol,2001

2. Dysembryoplastic neuroepithelial tumors located in the caudate nucleus area: Report of four cases;Cervera-Pierot;Neurosurgery,1997

3. Dysembryoplastic neuroepithelial tumours;Daumas-Duport;Brain Pathol,1993

4. Dysembryoplastic neuroepithelial tumor: A surgically curable tumor of young patients with intractable partial seizures;Daumas-Duport;Report of thirty-nine cases. Neurosurgery,1988

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