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osteochondroma/癲癇性発作

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8 結果

Giant intracranial osteochondroma: A case report and review of the literature.

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BACKGROUND Intracranial osteochondromas are uncommon. The majority of lesions arise from the base of the skull or from bones developed by endochondral ossification. A minority of cases are attached to the falxcerebri in the fronto parietal location. METHODS We report a case of a giant intracranial

February 2003: a 53-year-old male with new onset seizures.

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The February COM. A 53-year-old obese man presented with new onset seizures and an MRI scan revealed a large cystic and necrotic heterogeneously enhancing left frontal mass. Craniotomy revealed a firm subdural tumor on the cortical surface that was delivered en-bloc preserving the pial planes and

[Osteochondroma of the atlantooccipital joint. Extreme lateral transcondylar approach. A case description].

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BACKGROUND We describe a patient diagnosed as suffering from a skull base osteochondroma which affected the atlantooccipital joint and originated in the occipital condyle. It also displayed a growth toward the foramen magnum, which was resected using an extreme lateral transcondylar

Proximal chromosome 11p contiguous gene deletion syndrome phenotype: case report and review of the literature.

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The proximal chromosome 11p contiguous gene deletion syndrome (P11pDS), also known as Potocki-Shaffer syndrome (PSS) or DEFECT 11 (OMIM 601224), is a disorder associated with foramina parietalia permagna and multiple osteochondroma (exostoses). Additional features include mental retardation,

Multiple Exostoses Syndrome and Basilar Artery Aneurysm: A Case Report.

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Hereditary multiple exostoses (HME) is an inherited genetic condition, characterized by the formation of multiple osteochondromas, developing throughout childhood and into puberty. Vascular complications associated with HME are uncommon.A case of a patient

Long-term follow-up of four patients with Langer-Giedion syndrome: clinical course and complications.

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Long-term observations of individuals with the so-called Langer-Giedion (LGS) or tricho-rhino-phalangeal type II (TRPS2) are scarce. We report here a on follow-up of four LGS individuals, including one first described by Andres Giedion in 1969, and review the sparse publications on adults with this

Acrylic cranioplasty and axial pattern flap following calvarial and cerebral mass excision in a dog.

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A 4 kg Chihuahua was presented with seizures and a large mass on his dorsal cranium. The mass had regrown after two previous attempts to remove it. Histological examination had shown the mass to be a multilobular osteochondroma (osteochondrosarcoma). A CT scan revealed destruction of the dorsal

Transpterygoid approach to a dermoid cyst in pterygopalatine fossa.

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Objective To describe a case of dermoid cyst arising from the pterygopalatine fossa and review the literature. Methods We report a case of a 23-year-old man who suffered a car accident 2 years before otolaryngologic attendance. He had one episode of generalized tonic-clonic seizure and developed a
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