Atypical onset of sciatica in a patient with a filum terminale hemangioblastoma.
نویسندگان
چکیده
Hemangioblastomas are uncommon lesions that represent nearly 4% of the tumors of the spinal cord. Three fourths of them are sporadic, and the remainder are components of von Hippel Lindau (VHL) disease.1,2 They are mostly found in the cerebellum, although they can develop in the brain stem or spinal cord; of the latter, they are only rarely located in the filum terminale.3 The filum terminale is a delicate thread-like portion of fibrous tissue, a modification of the pia mater. It is about 20 cm long and originates at the vertex of the conus medullaris at the base of the coccyx, providing longitudinal support to the spinal cord.
منابع مشابه
Atypical Onset of Sciatica in a Patient With a Filum Terminale Hemangioblastoma Ciatalgia de presentación atípica en paciente con hemangioblastoma de filum terminale
Hemangioblastomas are uncommon lesions that represent nearly 4% of the tumors of the spinal cord. Three fourths of them are sporadic, and the remainder are components of von Hippel Lindau (VHL) disease.1,2 They are mostly found in the cerebellum, although they can develop in the brain stem or spinal cord; of the latter, they are only rarely located in the filum terminale.3 The filum terminale i...
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Filum terminale hemangioblastoma is an extremely rare tumour with only a few case reports in the literature. The natural history is unknown but benign as well as more aggressive presentations have been reported. The authors present the first such lesion discovered incidentally and discuss the available literature.
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Hemangioblastomas are benign tumours affecting the central nervous system (CNS) as sporadic case or as manifestation of von Hippel Lindau disease (VHL), a neoplastic multistemic autosomal dominant syndrome predisposing to develop CNS and visceral lesions. Hemangioblastomas are predominantly originating in the cerebellum and in the cervical and thoracic spinal cord; localization at the cauda equ...
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Paragangliomas are tumors arising from neuroepithelial cell groups called paraganglia, first reported by Alfred Kohn in 1903 [1]. They are benign tumors. The paraganglia are subdivided into two groups: one formed by the adrenal medulla and the other by the extraadrenal paraganglia. From the first one arises, the typical pheocromocytoma. The most common site for extra-adrenal paragangliomas is t...
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عنوان ژورنال:
- Reumatologia clinica
دوره 14 2 شماره
صفحات -
تاریخ انتشار 2018