Slow Spinal Cord Compression Inducing by Malignant Peripheral Nerve Sheath Tumors in Cotonou

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dc.contributor.authorGnonlonfoun, Dieudonnée
dc.contributor.authorADJIEN, KODJO CONSTANT
dc.contributor.authorMapaga, J. Nyangui
dc.contributor.authorHode, L.
dc.contributor.authorGoudjinou, Gérald
dc.contributor.authorSowanou, A
dc.contributor.authorDOMINGO, HUGUES RENAUD
dc.contributor.authorGnigone, P.
dc.contributor.authorMambila, G.
dc.contributor.authorAffanou, D.
dc.contributor.authorKouna Ndouongo, P. H.
dc.contributor.authorHouinato, Dismand
dc.date.accessioned2026-06-02T16:06:57Z
dc.date.available2026-06-02T16:06:57Z
dc.date.issued2018
dc.description.abstractMPNST is a very uncommon malignant type of neoplasm. It is often associated with neurofibromatosis type 1 (von Recklinghausen disease). It involves large anatomical regions, and thus takes on varied clinical presentations. However, bone location of MPNST, particularly in the spinal canal has been poorly described in the literature. We hereby report the case of a 29-year old young man with MPNST in the spinal canal. He presented a slow spinal cord compression confirmed by spinal MRI. MPNST was revealed through histologic and immune histochemical features after tumor resection.
dc.identifier.otherBECDB-6902
dc.identifier.urihttps://dspace.uac.bj/handle/123456789/6237
dc.language.isofr
dc.relation.ispartofNeuroscience & Medicine
dc.subjectSpinal Compression
dc.subjectMalignancy
dc.subjectMPNST
dc.subjectCotonou
dc.titleSlow Spinal Cord Compression Inducing by Malignant Peripheral Nerve Sheath Tumors in Cotonou
dc.typeArticle

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