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Words related to polyarteritis

inflammation of several arteries

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References in periodicals archive ?
Risk factors for rupture include pregnancy, polyarteritis nodosa, and noncalcified and symptomatic RAAs (3).
In his analysis of 60 patients with vasculitis associated with malignancy, Fain and colleagues (13) found cutaneous leukocytoclastic vasculitis (LV), polyarteritis nodosa (PAN), Churg-Strauss syndrome, microscopic polyangiitis, Wegener's granulomatosis, and Henoch-Schonlein purpura (HSP) to be triggered by malignancy.
Patients with renal involvement usually have hematuria, proteinuria, rapid progression of hypertension and worsening of renal function, with histological findings that are very similar to polyarteritis nodosa (Halpern & Citron, 1971).
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.
Even when a child has clinical findings that resemble "bite marks" or "ligature marks on hands and feet," missing fingernails, or tissue tears that suggest lacerations or avulsive injuries, the possibility of microscopic polyarteritis should be ruled out by tests for neutrophilia; lymphopenia; and elevated levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), Creactive protein (CRP), and lactate dehydrogenase (LDH) before accusing the caregiver of committing a crime.
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.
Visceral leishmaniasis in a patient treated for polyarteritis nodosa.
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.
Infections Atypical mycobacteria Bacterial - Streptococcus - Staphylococcus (especially MRSA) - Lyme borreliosis - Cutaneous anthrax - Syphilis - Gonococcemia - Ricketsial disease - Tularemia Deep Fungal - Sporotrichosis - Aspergillosis - Cryptococcosis Ecthyma gangrenosum (Pseudomonas aeruginosa) Parasitic (Leishmaniasis) Viral (herpes simplex, herpes zoster (shingles)) Vascular occlusive or venous disease Antiphospholipid-antibody syndrome Livedoid vasculopathy Small-vessel occlusive arterial disease Venous statis ulcer Necrotising vasculitis Leukocytoclastic vaculitis Polyarteritis nodosa Takayasu's arteritis Wegeners granulomatosis Neoplastic disease Leukemia cutis Lymphoma (e.
Cholesterol embolism: a multiple-system disease masquerading as polyarteritis nodosa.
Sometimes biopsies from patients with erythema induratum will show polyarteritis nodosa (PAN).
Nine chapters are new to this edition, on cytokine inhibitors, potential biologic therapies, pain mechanisms and management, vasculitis classification, Wegener's and anti-neutrophil cytoplasmic antibody-associated vasculitis, polyarteritis nodosa and microscopic polyarterities, hypersensitivity vasculitis, Behcet's syndrome, and other vasculitis syndromes.