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A case of rare lumbar intradural tumor: paraganglioma.
Sevin, Ismail Ertan; Dag, Onur Davut; Kahraman, Asli; Sucu, Hasan Kamil.
Afiliación
  • Sevin IE; Department of Neurosurgery, Izmir Katip Celebi University, Ataturk Training and Research Hospital, 35360 Izmir, Turkey.
  • Dag OD; Department of Neurosurgery, Izmir Katip Celebi University, Ataturk Training and Research Hospital, 35360 Izmir, Turkey.
  • Kahraman A; Department of Pathology, Izmir Katip Celebi University, Ataturk Training and Research Hospital, 35360 Izmir, Turkey.
  • Sucu HK; Department of Neurosurgery, Izmir Katip Celebi University, Ataturk Training and Research Hospital, 35360 Izmir, Turkey.
J Surg Case Rep ; 2024(2): rjae054, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38362492
ABSTRACT
Lumbar paragangliomas are rare neuroendocrine neoplasms arising from specialized neural crest cells in the cauda equina/filum terminale region. They are difficult to diagnose radiologically and can be difficult to treat surgically if they secrete catecholamines. A 38-year-old woman presented with three and a half years of increasing lower back and sacrum discomfort. Her neurological examination was normal. The MRI revealed an L4 intradural lesion that was compressing the cauda equina. A total tumor resection was conducted. The paraganglioma was diagnosed by the pathology report. Paragangliomas should be considered in the differential diagnosis of intradural masses of the lumbar spine.
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Texto completo: 1 Colección: 01-internacional Idioma: En Revista: J Surg Case Rep Año: 2024 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Idioma: En Revista: J Surg Case Rep Año: 2024 Tipo del documento: Article País de afiliación: Turquía