Myelitis due to Sjögren syndrome (Q88852): Difference between revisions
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Inflamação da medula espinal em associação com a síndrome de Sjogren, 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 clínicas da síndrome de Sjogren podem estar presentes, como a síndrome seca. 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 e teste sorológico para anticorpos associados à síndrome de Sjogren e biópsia de glândula lacrimal ou salivar. | |||
| description / en | description / en | ||
Inflammation of the spinal cord in association with Sjogren’s syndrome 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 clinical features of Sjogren’s syndrome may be present such as the sicca complex. Diagnosis may be aided by spinal imaging, spinal fluid analysis which may demonstrate a raised protein, lymphocytosis and the presence of oligoclonal bands and serological testing for antibodies associated with Sjogren’s syndrome and lacrimal or salivary gland biopsy. | |||
Revision as of 15:14, 15 August 2026
Inflammation of the spinal cord in association with Sjogren’s syndrome 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 clinical features of Sjogren’s syndrome may be present such as the sicca complex. Diagnosis may be aided by spinal imaging, spinal fluid analysis which may demonstrate a raised protein, lymphocytosis and the presence of oligoclonal bands and serological testing for antibodies associated with Sjogren’s syndrome and lacrimal or salivary gland biopsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1091662983 |
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| English | Myelitis due to Sjögren syndrome |
Inflammation of the spinal cord in association with Sjogren’s syndrome 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 clinical features of Sjogren’s syndrome may be present such as the sicca complex. Diagnosis may be aided by spinal imaging, spinal fluid analysis which may demonstrate a raised protein, lymphocytosis and the presence of oligoclonal bands and serological testing for antibodies associated with Sjogren’s syndrome and lacrimal or salivary gland biopsy. |
