Inflammatory polyneuropathy
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guillain-Barré syndrome) with the motor deficit reaching a maximal level by 28 days, and chronic inflammatory demyelinating polyneuropathy (CIDP) which has a slowly progressive course of two or more months or a relapsing remitting course. There are many variants of AIDP and CIDP.
sections/codes in this section (8C01-8C01)
- Acute inflammatory demyelinating polyneuropathy (8C01.0)
- Post vaccinal neuropathy (8C01.1)
- Subacute inflammatory demyelinating polyneuropathy (8C01.2)
- Chronic inflammatory demyelinating polyneuropathy (8C01.3)
- Other specified inflammatory polyneuropathy (8C01.Y)
- Inflammatory polyneuropathy, unspecified (8C01.Z)
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