The American College of Rheumatology 1990 criteria for the classification of polyarteritis
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.
Hanslik et al., "Development and validation of a consensus methodology for the classification of the ANCA-associated vasculitides and polyarteritis
nodosa for epidemiological studies," Annals of the Rheumatic Diseases, vol.
(3) dermatologic manifestations of systemic immunologic disorders, like scleroderma, polymyositis, and 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).
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.
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.