Polyarteritis nodosa (PAN) is a rare systemic disease marked by inflammation and tissue death in medium-sized arteries throughout the body, typically affecting the vessels supplying the kidneys and internal organs while characteristically sparing the lungs' circulation. As a medium-vessel vasculitis, PAN destroys arterial walls and produces a distinctive imaging finding, small aneurysms strung like the beads of a rosary, which helps distinguish it from other forms of vasculitis. The disease can damage multiple organ systems through reduced blood flow. It is associated with hepatitis B or C infection in some cases, though the cause is unknown in many others. With treatment, five-year survival is around 80 percent; without treatment, only about 13 percent survive five years.
Facts
Classification
ICD-10 ChapterXIII: Diseases of the Musculoskeletal System and Connective Tissue 2 Sources
1. Polyarteritis nodosa (Wikipedia)
lead sentence 1Quote, lead sentence 1
Polyarteritis nodosa (PAN) is a systemic necrotizing inflammation of blood vessels (vasculitis) affecting medium-sized muscular arteries, typically involving the arteries of the kidneys and other internal organs but generally sparing the lungs' circulation.
View the Source 2. World Health Organization: ICD-10 Version:2019 - M30.0
World Health OrganizationICD-10 2019 category M30.0, Chapter XIIIQuote, ICD-10 2019 category M30.0, Chapter XIII
M30.0 Polyarteritis nodosa
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