Inflammatory pachymeningitis (Q90281): Difference between revisions

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Paquimeningite hipertrófica devido a um processo inflamatório, incluindo sarcoidose, artrite reumatóide e vasculite. A síndrome é caracterizada por espessamento localizado ou difuso da dura-máter, embora todas as três membranas possam estar envolvidas. A dura-máter craniana, dura-máter espinhal ou ambas podem estar envolvidas. As características clínicas refletem a parte do neuroeixo afetada e podem incluir cefaleia, paralisia dos nervos cranianos, ataxia, paraparesia, perda sensitiva e perda do controle do esfíncter. O diagnóstico pode ser confirmado por neuroimagem, análise do líquido cefalorraquiano e biópsia meníngea.
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Hypertrophic pachymeningitis due to an inflammatory process including sarcoidosis, rheumatoid arthritis and vasculitis. The syndrome is characterised by localised or diffuse thickening of the dura mater, although all three membranes may be involved. 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 17:14, 15 August 2026

Hypertrophic pachymeningitis due to an inflammatory process including sarcoidosis, rheumatoid arthritis and vasculitis. The syndrome is characterised by localised or diffuse thickening of the dura mater, although all three membranes may be involved. 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.
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ID_2124989588
    English
    Inflammatory pachymeningitis
    Hypertrophic pachymeningitis due to an inflammatory process including sarcoidosis, rheumatoid arthritis and vasculitis. The syndrome is characterised by localised or diffuse thickening of the dura mater, although all three membranes may be involved. 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.

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