Myelitis due to haematobium (Q93801): Difference between revisions
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Doença inflamatória da medula espinal devido à infecção por Schistosoma haematobium. A parte inferior da medula espinhal geralmente é afetada. Os sintomas e sinais podem ser agudos ou subagudos no início e incluem paraparesia ou paraplegia, perda sensorial compatível com o nível da medula espinhal afetada, perda do controle dos esfíncteres e síndrome do neurônio motor inferior. O diagnóstico pode ser confirmado por neuroimagem, análise do líquido espinal, testes sorológicos e biópsia. | |||
| description / en | description / en | ||
An inflammatory disorder of the spinal cord due to infection by a Schistosoma haematobium. The lower spinal cord is usually affected. The symptoms and signs may be acute or subacute in onset, and include paraparesis or paraplegia, sensory loss appropriate with the level of the spinal cord affected, loss of sphincter control, and lower motor neurone signs. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis, serological tests, and biopsy. | |||
Revision as of 08:54, 16 August 2026
An inflammatory disorder of the spinal cord due to infection by a Schistosoma haematobium. The lower spinal cord is usually affected. The symptoms and signs may be acute or subacute in onset, and include paraparesis or paraplegia, sensory loss appropriate with the level of the spinal cord affected, loss of sphincter control, and lower motor neurone signs. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis, serological tests, and biopsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1291371639 |
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| English | Myelitis due to haematobium |
An inflammatory disorder of the spinal cord due to infection by a Schistosoma haematobium. The lower spinal cord is usually affected. The symptoms and signs may be acute or subacute in onset, and include paraparesis or paraplegia, sensory loss appropriate with the level of the spinal cord affected, loss of sphincter control, and lower motor neurone signs. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis, serological tests, and biopsy. |
