The American College of Rheumatology 1990 criteria for the classification of
polyarteritis nodosa.
Case number 34: Relapse of
polyarteritis nodosa presenting as isolated and localised lower limb periostitis.
Segelmark, "Incidence and survival rates in Wegener's granulomatosis, microscopic polyangiitis, Churg-Strauss syndrome and
polyarteritis nodosa," Rheumatology, vol.
Bonfils, "Sudden bilateral hearing loss revealing
polyarteritis nodosa," European Annals of Otorhinolaryngology, Head and Neck Diseases, vol.
(3) dermatologic manifestations of systemic immunologic disorders, like scleroderma, polymyositis, and
polyarteritis nodosa
In
polyarteritis nodosa and lupus, mesenteric infarction may arise, having rectorrhagia as late clinical expression (Shirai et al 2013).
EULAR/PRINTO/PRES criteria for HenochSchonlein purpura, childhood
polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008.
Extrahepatic manifestations Several extrahepatic manifestations, including vasculitis, purpura, mixed cryoglobulinemia,
polyarteritis nodosa, arthralgias, glomerulonephritis, peripheral neuropathy, have been reported in CHB patients (1, 2).
(1,2)
Polyarteritis nodosa should be considered as a possible diagnosis in patients with HSP who have an unusual course, especially in patients presenting with severe neurological complications.
Polyarteritis is a multisystemic panarteritis involving medium-sized and small arteries.
Deaths occurring during the first year after treatment onset for
polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss syndrome: A retrospective analysis of causes and factors predictive of mortality based on 595 patients.