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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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:
Case Report
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
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author Traore, Wend-Yam Mohamed
Merbouh, Sahar
Diallo, Ibrahima Dokal
Cherif, Kettani Ech
Jiddane, Mohamed
Touarsa, Firdous
author_facet Traore, Wend-Yam Mohamed
Merbouh, Sahar
Diallo, Ibrahima Dokal
Cherif, Kettani Ech
Jiddane, Mohamed
Touarsa, Firdous
author_sort Traore, Wend-Yam Mohamed
collection PubMed
description 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.
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spelling pubmed-103363492023-07-13 A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report Traore, Wend-Yam Mohamed Merbouh, Sahar Diallo, Ibrahima Dokal Cherif, Kettani Ech Jiddane, Mohamed Touarsa, Firdous Radiol Case Rep 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.” 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. Elsevier 2023-07-01 /pmc/articles/PMC10336349/ /pubmed/37448607 http://dx.doi.org/10.1016/j.radcr.2023.06.032 Text en © 2023 Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Traore, Wend-Yam Mohamed
Merbouh, Sahar
Diallo, Ibrahima Dokal
Cherif, Kettani Ech
Jiddane, Mohamed
Touarsa, Firdous
A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
title A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
title_full A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
title_fullStr A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
title_full_unstemmed A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
title_short A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
title_sort spinal cord compression syndrome revealing neurofibromatosis type 1: a case report
topic Case Report
url 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
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