4A44.4 Polyarteritis nodosa
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Polyarteritis nodosa is an immunologically mediated systemic necrotising vasculitis affecting medium-sized vessels. In a few cases, the disease appears after viral infection but in the majority of cases there is no known triggering event. The clinical manifestations involve numerous organs and lead to a general alteration in the health status including rapid weight loss, paralysis of the peripheral nerves, renal disease, and digestive problems such as haemorrhages, perforation, appendicitis and pancreatitis. Arthralgia is almost always present and myalgia occurs in half of patients. Cardiac and cerebral anomalies (cephalalgia) are also reported, as well as ocular and genital (orchitis) manifestations.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Polyarteritis nodosa
- panarteritis nodosa
- periarteritis nodosa
- Kussmaul disease
- PAN - [polyarteritis nodosa]
- polyangiitis
- panangiitis
- arteritis nodosa
- Polyneuropathy in polyarteritis nodosa
- Periarteritis nodosa with necrosis
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