Myelitis due to Behcet’s disease (Q88853): Difference between revisions
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Inflamação da medula espinal em associação com a doença de Behçet, que pode ser temporalmente aguda, subaguda ou crônica e anatomicamente parcial ou completa. Manifestações clínicas incluem paraplegia, tetraplegia, perda sensitiva correspondente ao nível da medula espinal envolvida e disfunção esfincteriana. Outras manifestações neurológicas ou sistêmicas da doença de Behçet podem estar presentes. O diagnóstico pode ser auxiliado por exames de imagem da medula espinal, análise do líquido cefalorraquidiano que pode demonstrar uma proteína elevada, linfocitose e a presença de bandas oligoclonais, teste de patergia e teste de HLA. | |||
| description / en | description / en | ||
Inflammation of the spinal cord in association with Behcet’s disease which may be temporally acute, subacute or chronic and anatomically partial or complete. Clinical features include paraplegia, quadriplegia, sensory loss appropriate to the level of the spinal cord involved and sphincter dysfunction. Other neurological or systemic features of Behcet’s disease may be present. Diagnosis may be aided by spinal imaging, spinal fluid analysis which may demonstrate a raised protein, lymphocytosis and the presence of oligoclonal bands, pathergy testing and HLA testing. | |||
Revision as of 15:14, 15 August 2026
Inflammation of the spinal cord in association with Behcet’s disease which may be temporally acute, subacute or chronic and anatomically partial or complete. Clinical features include paraplegia, quadriplegia, sensory loss appropriate to the level of the spinal cord involved and sphincter dysfunction. Other neurological or systemic features of Behcet’s disease may be present. Diagnosis may be aided by spinal imaging, spinal fluid analysis which may demonstrate a raised protein, lymphocytosis and the presence of oligoclonal bands, pathergy testing and HLA testing.
| Language | Label | Description | Also known as |
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| default for all languages | ID_2069261453 |
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| English | Myelitis due to Behcet’s disease |
Inflammation of the spinal cord in association with Behcet’s disease which may be temporally acute, subacute or chronic and anatomically partial or complete. Clinical features include paraplegia, quadriplegia, sensory loss appropriate to the level of the spinal cord involved and sphincter dysfunction. Other neurological or systemic features of Behcet’s disease may be present. Diagnosis may be aided by spinal imaging, spinal fluid analysis which may demonstrate a raised protein, lymphocytosis and the presence of oligoclonal bands, pathergy testing and HLA testing. |
