Inflammatory polyneuropathy (Q41360): Difference between revisions
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Neuropatias periféricas inflamatórias adquiridas são de etiologia imune presumida e são classificadas com base em seu curso clínico: polineuropatia inflamatória desmielinizante aguda (PIDA ou síndrome de Guillain-Barré) com o déficit motor atingindo um nível máximo em 28 dias e polineuropatia inflamatória desmielinizante crônica (PIDC) que tem um curso lentamente progressivo de dois ou mais meses ou um curso remitente recorrente. Existem muitas variantes de PIDA e PIDC. | |||
| description / en | description / en | ||
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. | |||
Revision as of 07:29, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C01 |
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| English | Inflammatory polyneuropathy |
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. |
