Dysembryoplastic Neuroepithelial Tumor (DNT): Morphological and Immunohistochemical Features

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Dysembryoplastic Neuroepithelial Tumor (DNT): Morphological and Immunohistochemical Features

Dysembryoplastic neuroepithelial tumor is a rare mixed neuronalglial tumor. The recognition and correct diagnosis of dysembryoplastic neuroepithelial tumor is important because this tumor is curable by excision. The records of the Pathology Department at King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia, were reviewed for cases that were histologically diagnosed as dysem...

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Dysembryoplastic Neuroepithelial Tumor: A Review

BARROW QUARTERLY • Vol. 24, No. 1 • 2008 Dysembryoplastic Neuroepithelial Tumor: A Review I 1988 Dumas-Duport et al. first used the term dysembryoplastic neuroepithelial tumor to describe low-grade tumors found in young patients with intractable partial seizures.4 In 1993 the distinct pathological entity known as DNET was given a place in the WHO classification of brain tumors as a grade I tumo...

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Dysembryoplastic neuroepithelial tumor: A rare case report

Dysembryoplastic neuroepithelial tumor and adolescents with intractable epilepsy. This tumor demonstrates typical histological features such as glial nodules and the so called imaging features but needs a multidisciplinary contribution from the clinical and diagnostic department involving the clinician, radiologist as well as the pathologist to reach a definite an conclusive diagnosis. However ...

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Dysembryoplastic Neuroepithelial Tumors.

Dysembryoplastic neuroepithelial tumor (DNT) is a benign glioneuronal neoplasm that most commonly occurs in children and young adults and may present with medically intractable, chronic seizures. Radiologically, this tumor is characterized by a cortical topography and lack of mass effect or perilesional edema. Partial complex seizures are the most common presentation. Three histologic subtypes ...

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ژورنال

عنوان ژورنال: Journal of King Abdulaziz University-Medical Sciences

سال: 2007

ISSN: 1319-1004,1658-4279

DOI: 10.4197/med.14-3.5