8E41.1ICD-11 MMS 2026-01
Idiopathic hypertrophic pachymeningitis
Description
Inflammation of the pachymeninges resulting in localised or diffuse thickening of the dura mater for which no identifiable cause is found. The cranial and/or the spinal dura may be affected. Neurological features include headache, visual disturbance, cranial nerve palsies, ataxia and with spinal involvement, limb weakness, sensory impairment and sphincter disturbances. Diagnosis may be aided by neuroimaging and spinal fluid analysis and dural biopsy.
Index terms
- Idiopathic hypertrophic pachymeningitis
Exclusions from above levels
05– Endocrine, nutritional or metabolic diseases18– Complications of pregnancy, childbirth and the puerperium19– Certain conditions originating in the perinatal period
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22– Injury, poisoning or certain other consequences of external causes
Sibling codes
Foundation entity
Idiopathic hypertrophic pachymeningitis – http://id.who.int/icd/entity/2114942178
Allowed postcoordination axes
Part of: 8E41: Pachymeningitis › 08: Diseases of the nervous system