PAN

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Related to polyarteritis nodosa: polyarthritis, Wegener's granulomatosis, vasculitis

PAN

GOST 7.67 Latin three-letter geocode for Panama. The code is used for transactions to and from Panamanian bank accounts and for international shipping to Panama. As with all GOST 7.67 codes, it is used primarily in Cyrillic alphabets.
References in periodicals archive ?
Table 1 Prevalence of ANCA Positivity in Rheumatic Diseases C-ANCA C-ANCA P-ANCA (% positive) (% positive) Wegener's granulomatosis 85 10 Microscopic polyangiitis (MPA) 15-45 45-80 Renal-limited MPA 25 65 Churg-Strauss granulomatosis 10 60 Polyarteritis nodosa 5 15 Table 2 Clinical Trials Induction Maintenance CYCLOPS (a) CYCAZEREM (e) NORAM (b) IMPROVE (f) MEPEX (c) WEGET (g) RITUXIMAB (d) Co-TRIMOXAZOLE (h) (a) Cyclophosphamide (CYT) Oral vs Intravenous Pulses.
Adu D, Bacon PA: Classical polyarteritis nodosa, microscopic polyarteritis, and Churg-Strauss syndrome.
Owen J, Hauth JC: Polyarteritis nodosa in pregnancy: a case report and brief literature review.
Melin JP, Lemaire P, Birembaut P, et al: Polyarteritis nodosa with bilateral ureteric involvement.
Since he had ongoing constitutional symptoms with negative serology and cultures, a conventional mesenteric artery angiography was performed to rule out polyarteritis nodosa.
Presentation and outcome of gastrointestinal involvement in systemic necrotizing vasculitides: analysis of 62 patients with polyarteritis nodosa, microscopic polyangiitis, Wegener granulomatosis, Churg-Strauss syndrome, or rheumatoid arthritis-associated vasculitis.
We report the case of a 65-year-old man who was diagnosed to have polyarteritis nodosa having presented atypically with hematuria.
Cutaneus polyarteritis nodosa is a variant of polyarteritis nodosa (PAN), without visceral involvement and with a more favourable prognosis.
Key words: Cutaneus polyarteritis nodosa, differential diagnosis, systemic corticosteroids
Headache with systemic illness (fever, stiff neck, rash) may reflect meningitis, encephalitis, lyme disease, systemic infection, or collagen vascular diseases such as rheumatoid arthritis, systemic lupus erythematosus, scleroderma, polyarteritis nodosa, and dermatomyositis.
3[degrees]C at screening Immune modifying medications: Anti-inflammatory agents, Antibiotics, Steroids Subjects with any history of immune system disorder or auto-immune disorder including but not limited to the following: * AIDS, HIV, * Ankylosing Spondylitis, Chronic Fatigue Syndrome, CREST Syndrome, Crohn's Disease, Dermatomyositis, Fibromyalgia, Grave's Disease, Hashimoto's Thyroiditis, Lupus, Myasthenia Gravis, Pernicious Anemia, Polyarteritis Nodosa, Primary Biliary Cirrhosis, Psoriasis, Reynaud's Disease, Rheumatoid Arthritis, Sarcoidosis, Scleroderma, Sjogren's Syndrome, Temporal Arthritis, Ulcerative Colitis, and Vitiligo Use of any immunosuppressive drugs in the last 5 years (Steroids, Biologics, etc.
5-8) Miscellaneous extrahepatic manifestations (glomerulonephritis, polyarteritis nodosa, cryoglobulinemia, thrombocytopenia, agranulositosis, aplastic anemia, pancreatitis) are seen in 6.