cutaneous polyarteritis nodosa

Mutations in the CERC1 gene associated with deficiency of ADA2 protein have been implicated in the pathogenesis of cPAN and early-onset vasculopathy. Cutaneous polyarteritis nodosa (cPAN) is a benign ... The New England Journal of Medicine: Treatment of Parvovirus B19–Associated Polyarteritis Nodosa with Intravenous Immune Globulin We describe a patient who had polyarteritis nodosa associated with parvovirus B19 infection that regressed completely with intravenous immune globulin therapy.

Understanding the Context

A 33-year-old woman was seen because of ... Polyarteritis nodosa vasculopathy may be caused by recessive loss-of-function mutations in a single gene (CECR1) encoding adenosine deaminase 2 (ADA2), a finding with potential clinical implications, ... Nature: Polyvisceral arteritis in chronic graft-versus-host disease: antiphospholipid-negative thrombotic syndrome mimicking polyarteritis nodosa Polyvisceral arteritis in chronic graft-versus-host disease: antiphospholipid-negative thrombotic syndrome mimicking polyarteritis nodosa Polyarteritis nodosa (PAN) is a rare disease that makes your blood vessels swell. It can affect the blood vessels that go to almost every part of your body, including your heart, kidneys, and ...