Hypertrophic pachymeningitis (Q97636): Difference between revisions
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Paquimeningite hipertrófica é caracterizada por espessamento localizado ou difuso da dura-máter. Pode ser idiopática ou secundária a transtornos inflamatórios, infecções, transtornos imunomediados e doenças malignas. A dura-máter craniana, dura-máter espinal ou ambas podem estar envolvidas. As manifestações clínicas refletem a parte do neuroeixo afetada e podem incluir cefaleia, paralisia de nervos cranianos, ataxia, paraparesia, perda sensorial e perda do controle esfincteriano. O diagnóstico pode ser confirmado por neuroimagem, análise do líquido cefalorraquiano e biópsia meníngea. | |||
| description / en | description / en | ||
Hypertrophic pachymeningitis is characterised by localised or diffuse thickening of the dura mater. It may be idiopathic or secondary to inflammatory disorders, infections, immune-mediated disorders and malignancies. The cranial dura, spinal dura or both may be involved. The clinical features reflect the part of the neuraxis affected and may include headache, cranial nerve palsies, ataxia, paraparesis, sensory loss and loss of sphincter control. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis and meningeal biopsy. | |||
Revision as of 13:45, 16 August 2026
Hypertrophic pachymeningitis is characterised by localised or diffuse thickening of the dura mater. It may be idiopathic or secondary to inflammatory disorders, infections, immune-mediated disorders and malignancies. The cranial dura, spinal dura or both may be involved. The clinical features reflect the part of the neuraxis affected and may include headache, cranial nerve palsies, ataxia, paraparesis, sensory loss and loss of sphincter control. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis and meningeal biopsy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1561437485 |
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| English | Hypertrophic pachymeningitis |
Hypertrophic pachymeningitis is characterised by localised or diffuse thickening of the dura mater. It may be idiopathic or secondary to inflammatory disorders, infections, immune-mediated disorders and malignancies. The cranial dura, spinal dura or both may be involved. The clinical features reflect the part of the neuraxis affected and may include headache, cranial nerve palsies, ataxia, paraparesis, sensory loss and loss of sphincter control. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis and meningeal biopsy. |
