Meningitis due to Behçet disease (Q96547): Difference between revisions
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Inflamação das meninges devido à doença de Behçet. A síndrome é clinicamente caracterizada por cefaleia, rigidez de nuca, febre e fotofobia. A apresentação pode ser aguda, subaguda, crônica ou recorrente. Outras características clínicas da doença de Behçet, neurológicas e não neurológicas, podem estar presentes. O diagnóstico pode ser auxiliado por neuroimagem, teste de patergia e teste HLA. A análise do líquido cefalorraquiano pode revelar uma pleocitose linfocítica, proteína elevada e a presença de bandas oligoclonais. | |||
| description / en | description / en | ||
Inflammation of the meninges due to Behcet’s disease. The syndrome is clinically characterised by headache, neck stiffness, fever and photophobia. The presentation may be acute, subacute, chronic or recurrent. Other clinical features of Behcet’s disease, both neurological and non-neurological, may be present. Diagnosis may be aided by neuroimaging, pathergy testing and HLA testing. Spinal fluid analysis may reveal a lymphocytic pleocytosis, raised protein and the presence of oligoclonal bands. | |||
Revision as of 12:34, 16 August 2026
Inflammation of the meninges due to Behcet’s disease. The syndrome is clinically characterised by headache, neck stiffness, fever and photophobia. The presentation may be acute, subacute, chronic or recurrent. Other clinical features of Behcet’s disease, both neurological and non-neurological, may be present. Diagnosis may be aided by neuroimaging, pathergy testing and HLA testing. Spinal fluid analysis may reveal a lymphocytic pleocytosis, raised protein and the presence of oligoclonal bands.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_495560646 |
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| English | Meningitis due to Behçet disease |
Inflammation of the meninges due to Behcet’s disease. The syndrome is clinically characterised by headache, neck stiffness, fever and photophobia. The presentation may be acute, subacute, chronic or recurrent. Other clinical features of Behcet’s disease, both neurological and non-neurological, may be present. Diagnosis may be aided by neuroimaging, pathergy testing and HLA testing. Spinal fluid analysis may reveal a lymphocytic pleocytosis, raised protein and the presence of oligoclonal bands. |
