نتایج جستجو برای: Cerebellar Astrocytoma

تعداد نتایج: 35156  

A Ebrahimi Nezhad A. R Malek Pour

Cerebellar pilocytic Astrocytoma is a benign tumor, acounts for 80% of all cerebellar Astrocytoma, and has a relatively good prognosis. This tumor usually presents with Ataxia and in the case of hydrocephaly with raised intracranial pressure signs such as headeach, and vomiting. Treatment of this tumor is complete resection and if hydrocephally is present V.P. shunt should be inserted. In the c...

Journal: :East and Central African Journal of Surgery 2017

ژورنال: پژوهش در پزشکی 2019

Abstract Background: Cerebellar tumors are considered as clinically significant intracranial neoplasms and acknowledgment of their epidemiological characteristics tends to be essential. The present study was conducted in order to determine the prevalence and types of their cerebellar tumors in Shohada-e-Tajrish Hospital between 2006-2014. Materials and Methods: In the current observational...

Journal: :Pediatrics 1956
D D MATSON

150 I T IS GENERALLY appreciated that modulloblastoma, perhaps the most rapidly growing and highly malignant of all brain neoplasms, commonly involves the corebelhum and fotmrth ventricle of young children. Umifortimnatoly, the gloomy outlook for this tumor has too often spread to encompass all brain tumors in childhood and overshadow the fact that cerebollar astrocytoma, a tuITlO at the opposi...

2015
Somnath Sharma Bal Krishan Ojha Anil Chandra Sunil Kumar Singh Chhitij Srivastava Preeti Agarwal Kalpana Sharma

Pilomyxoid astrocytomas (P.M.A) are new class of Pilocytic Astrocytoma (P.A.) which typically have their origin in hypothalamus and chiasmatic region. There are very few case reports of PMAs arising from cerebellum. Their imaging features are similar to PA but they behave more aggressively than PA. The authors report a case of 10 year old male child who presented with right cerebellar tumour di...

2016
Ebtissam Alerraqi

Neurologically, BRAF V600E mutation was detected in cerebellar anaplastic pilocytic astrocytoma [6], ganglioglioma [7], desmoplastic infantile astrocytoma [8], indeterminate cell tumor and interdigitating dendritic cell sarcoma [9]. Hematologically, BRAF V600E mutation was also detected in multiple myeloma [10] and several leukemias (hairy cell, chronic lymphocytic, prolymphocytic and acute lym...

2016

Abstract Gliomas of the cerebellum are rare in adults, and their natural history and clinical behavior are not well known. Because cerebellar glioma is not usually diagnosed until clinical symptoms have appeared, no reports have described the developmental process of new cerebellar gliomas. We describe a case of de novo cerebellar anaplastic astrocytoma in which the developmental process was de...

Journal: :Revista de neurologia 2009
M R P Freitas S D C de Muzio R C C Pessoa J N Stávale L R R Borges S M F Malheiros

INTRODUCTION Cerebellar high-grade astrocytoma is uncommon. Although more prone to present cerebrospinal fluid dissemination, the cerebellar location is not particularly related to the occurrence of extra-cranial metastases, which are also unusual in supratentorial malignant gliomas. CASE REPORT A 46 year-old man with cerebellar anaplastic astrocytoma who developed pancytopenia due to extensi...

Journal: :Journal of neurosurgery 2013
Atsushi Kanoke Masayuki Kanamori Toshihiro Kumabe Ryuta Saito Mika Watanabe Teiji Tominaga

This patient presented with a rare case of metachronous, multicentric gliomas first manifesting as headache and nausea in 1983 when he was an 8-year-old boy. Computed tomography revealed a cerebellar tumor and the tumor was subtotally resected. The histological diagnosis was pilocytic astrocytoma, and radiation therapy to the posterior fossa and chemotherapy consisting of nimustine hydrochlorid...

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