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A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report

Neurofibromatosis type 1 (NF1), formerly known as von Recklinghausen disease is an autosomal dominant disease with multisystem involvement. In the peripheral nervous system, it leads to the development of benign tumors from the tissue of the spinal or cranial nerve sheaths, known as “neurofibromas.”...

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Detalles Bibliográficos
Autores principales: Traore, Wend-Yam Mohamed, Merbouh, Sahar, Diallo, Ibrahima Dokal, Cherif, Kettani Ech, Jiddane, Mohamed, Touarsa, Firdous
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336349/
https://www.ncbi.nlm.nih.gov/pubmed/37448607
http://dx.doi.org/10.1016/j.radcr.2023.06.032
Descripción
Sumario:Neurofibromatosis type 1 (NF1), formerly known as von Recklinghausen disease is an autosomal dominant disease with multisystem involvement. In the peripheral nervous system, it leads to the development of benign tumors from the tissue of the spinal or cranial nerve sheaths, known as “neurofibromas.” We report the case of a 40-year-old patient with spinal cord compression syndrome in whom spinal MRI revealed cervical, dorsal and lumbosacral neurofibromas revealing neurofibromatosis type 1.