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Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor in the Cerebellopontine Angle : Diagnosis and Treatment
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-188482
Biblioteca responsável: WPRO
ABSTRACT
Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) is an unusual malignancy with aggressive behavior. ES/PNET in the cerebellopontine angle (CPA) is extremely uncommon, and we report on a rare case here. A 31-year-old man presented with one month history of left facial palsy, hearing loss, swallowing difficulty, and hoarseness. Magnetic resonance images showed a large mass in the left CPA and a small one in the right cerebellar hemisphere. The patient underwent a surgery for the CPA mass lesion, and the pathology was compatible with ES/PNET. Radiation therapy and chemotherapy were administered. In contrast to the initial radiologic findings resembling vestibular schwannoma or meningioma, ES/PNET had several distinct clinical features. A patient with a CPA mass and presenting unusual clinical features should be suspected of having a rare malignancy.
Assuntos

Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Sarcoma de Ewing / Espectroscopia de Ressonância Magnética / Rouquidão / Neuroma Acústico / Ângulo Cerebelopontino / Tumores Neuroectodérmicos / Tumores Neuroectodérmicos Primitivos / Deglutição / Paralisia Facial / Perda Auditiva Tipo de estudo: Estudo diagnóstico Limite: Adulto / Humanos Idioma: Inglês Revista: Journal of Korean Neurosurgical Society Ano de publicação: 2011 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Sarcoma de Ewing / Espectroscopia de Ressonância Magnética / Rouquidão / Neuroma Acústico / Ângulo Cerebelopontino / Tumores Neuroectodérmicos / Tumores Neuroectodérmicos Primitivos / Deglutição / Paralisia Facial / Perda Auditiva Tipo de estudo: Estudo diagnóstico Limite: Adulto / Humanos Idioma: Inglês Revista: Journal of Korean Neurosurgical Society Ano de publicação: 2011 Tipo de documento: Artigo
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