نتایج جستجو برای: sub ependymal giant cell astrocytoma

تعداد نتایج: 1925277  

1993
James T. Rutka Sherri Lynn Smith

Glial fibrillary acidic protein (GFAP) is a A/, 50,000 intracytoplasmic filamentous protein that constitutes a portion of, and is spécifiefor the cytoskeleton of the astrocyte. GFAP appears to stabilize the astrocyte's cytoskeleton, and helps maintain normal astrocyte cell shape through complex interactions between it and the nuclear and plasma membranes. A critical observation from histopatho...

Journal: :The American journal of surgical pathology 2013
Bette Kay Kleinschmidt-DeMasters Dara L Aisner Diane K Birks Nicholas K Foreman

BRAF V600E mutation has been identified in up to 2/3 of pleomorphic xanthoastrocytomas (PXAs), World Health Organization grade II, as well as in varying percentages of PXAs with anaplastic features (PXA-A), gangliogliomas, extracerebellar pilocytic astrocytomas, and, rarely, giant cell glioblastoma multiforme (GC-GBMs). GC-GBMs and epithelioid GBMs (E-GBMs) can be histologically challenging to ...

Journal: :Journal of pediatric hematology/oncology 2014
Dolly Aguilera Robert Flamini Claire Mazewski Matthew Schniederjan Laura Hayes William Boydston Robert C Castellino Tobey J MacDonald

BACKGROUND Brain subependymal giant cell astrocytomas (SEGAs) in patients with tuberous sclerosis have been reported to respond to everolimus. METHODS A 15-year-old male patient with intractable seizures and multiple SEGAs of the brain developed leptomeningeal enhancement and multiple metastatic, histologically confirmed SEGAs of the spinal cord. He received daily everolimus at a dose of 3 mg...

Journal: :Chinese journal of cancer research = Chung-kuo yen cheng yen chiu 2011
Peng-Fei Ge Hai-Feng Wang Li-Mei Qu Bo Chen Shuanglin Fu Yinan Luo

Pilomyxoid astrocytoma is a new identified variant type of pilocytic astrocytoma, and typically locates in the hypothalamic and chiasmatic region. Herein, we reported a nine-year-old boy with pilomyxoid astrocytoma in the cerebellum. MRI scanning showed a tumor involved the cerebellar vermis, tonsil, the forth ventricle and brainstem. It was homogeneous isointensity on T1WI, relative hyper-inte...

  Two rare cases of extra-articular diffuse variant giant cell tumor of the tendon sheath are presented, at the elbow of a 68-year-old female and the foot of a 56-year-old male. Both patients presented with a palpable masses and marginal excision was performed; histological sections confirmed the diagnosis of extra-articular giant cell tumor. No adjuvant therapy was administered. At the last fo...

2013
Khaled M. Krisht Meic H. Schmidt

Tanycytic ependymoma is a rare form of ependymoma that usually arises in the intramedullary spine. It has a unique histology emphasized by the inconspicuous ependymal pattern of cells and close resemblance to schwannoma and astrocytoma. The authors report a 50-year-old man with a cervical tanycytic ependymoma that was initially thought to be a schwannoma. The frozen histology section showed spi...

2015
Laura F. Corns Lucy Atkinson Jill Daniel Ian J. Edwards Lauryn New Jim Deuchars Susan A. Deuchars

The region surrounding the central canal (CC) of the spinal cord is a highly plastic area, defined as a postnatal neurogenic niche. Within this region are ependymal cells that can proliferate and differentiate to form new astrocytes and oligodendrocytes following injury and cerebrospinal fluid contacting cells (CSFcCs). The specific environmental conditions, including the modulation by neurotra...

1999
R Nabbout M Santos Y Rolland O Delalande O Dulac C Chiron

Objectives—Intraventricular astrocytomas (subependymal giant cell astrocytomas) of tuberous sclerosis have a poor prognosis due to the obstruction of CSF flow. The aim of this study was to determine whether they could be diVerentiated during childhood and at an early preclinical stage, from subependymal nodules without any growing potential. Methods—The first two MRIs of all children referred t...

Journal: :The Lancet. Neurology 2015
Paolo Curatolo Romina Moavero Petrus J de Vries

Tuberous sclerosis (also known as tuberous sclerosis complex [TSC]) is a multisystem genetic disorder that affects almost every organ in the body. Mutations in the TSC1 or TSC2 genes lead to disruption of the TSC1-TSC2 intracellular protein complex, causing overactivation of the mammalian target of rapamycin (mTOR) protein complex. The surveillance and management guidelines and clinical criteri...

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