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13 resultats
An Intracerebral Type of Cranial Chondroma.
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The vast majority of intracranial chondromas are located in the base of the cranium. Their presentation as an intracerebral neoplasm is considered to be extremely rare. A previously healthy 45-year-old man experienced recurrent seizure attacks over a period of 6 months. Imaging studies of the brain
Giant Dural Supratentorial Chondroma Generating the Question of How Large Can a Tumor Become Without Revealing Itself.
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Chondromas usually affect the small bones of hand and feet and account for only 0.5% of all intracranial tumors. We present a case of a giant, supratentorial meningeal chondroma in a 19-year old male patient and discuss the preoperative diagnostic findings as well as the appropriate treatment
Cystic falcine chondroma: case report and review of the literature.
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A rare case of falcine chondroma in a 25-year-old woman with an 8-year history of headache and a recent generalized seizure is presented. Microscopic examination of the resected tumor revealed that it was a falcine chondroma with chondrocytes and central cystic degeneration.
Skull Base Enchondroma and Chondrosarcoma in Ollier Disease and Maffucci Syndrome.
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Large chondroma of the dural convexity in a patient with Noonan's syndrome. Case report and review of the literature.
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BACKGROUND
Intracranial chondromas are extremely rare intracranial tumours that usually arise from the skull base synchondrosis. Exceptionally, they may grow from cartilage rests within the dura mater of the convexity or the falx. They may be part of Ollier's multiple enchondromatosis or Maffuci's
Giant convexity chondroma with meningeal attachment.
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OBJECTIVE
Intracranial chondroma is a rare and benign tumor with usual onset in young adulthood. The skull base is the most common site of occurrence although, less often, the tumors can appear at the falx cerebri or at the dural convexity. The differentiation of these lesions from meningiomas
Choroid plexus papilloma with chondroma: case report.
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The authors report the successful total removal of a rare intracranial tumor in the right lateral ventricle of a 15-year-old girl with epileptic seizures. Histopathological examination showed a benign tumor formed by mature cartilage and choroid plexus papilloma. From our review of the literature, a
Chondromatosis of the choroid plexus.
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A case of chondromatosis of the choroid plexus in a 19 year old woman presenting with focal seizures is reported. Benign intracranial cartilaginous lesions are reviewed and the differential diagnosis of chondromatosis of the choroid plexus and intraventricular chondromas discussed.
A Case of Ollier's Disease with P53 Mutation Positive and IDH1 (R132H) Negative Multicentric Gliomas
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Ollier disease is a rare nonhereditary disorder characterized by multiple enchondromas (enchondromatosis). To report a rare case of Ollier disease with gliomas and its mutation analysis. We hereby report a young lady who presented with seizures. She had a past history of multiple bony swellings in
Ollier's disease and Maffucci's syndrome: distinct entities or a continuum. Case report: enchondromatosis complicated by an intracranial glioma.
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A patient with the diagnosis of enchondromatosis (Ollier's disease) presented with seizures. CT examination showed an avascular right frontal lobe lesion. Surgery revealed a histologically verified grade II astrocytoma. This case is consistent with recent evidence that questions the distinction
Intracranial extraskeletal myxoid chondrosarcoma: case report and review of the literature.
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BACKGROUND
We describe a patient with an intracranial extra skeletal myxoid chondrosarcoma (EMC), an unusual neoplasm of the deep soft tissues of the extremities. Very rarely are they localised as an intracranial lesion, and we believe it is very important to accurately distinguish EMC from other
Parafalcine chondrosarcoma: an unusual localization for a classical variant. Case report and review of the literature.
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BACKGROUND
Intracranial chondroid tumors are infrequently seen in neurosurgical practice. These tumors usually arise from cartilaginous synchondroses at the base of the skull, but occasionally from the pluripotential mesenchymal cells of the meninges. We present here a case of classic low-grade
[A broad subfrontal access to the tumors in the base of the skull].
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A total of 30 patients, aged 16 to 67, with neoplasms in the brain base and in paranasal sinuses were operated on, during 1997-2002, at Burdenko's Research Institute for Neurosurgery of the Russian Academy of Medical Sciences (RAMS). A majority of patients (21) had meningiomas. Other observations
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