Polyarteritis nodosa presenting as bilateral sudden onset cochleo-vestibular failure in a young woman.
Computed tomography (CT) abnormalities leading to CT-initiated exclusion from kidney donation in 81 patients n Collecting system 41 Renal calculi 39 Ureteropelvic junction obstruction 2 due to crossing vessels Renal vasculature 29 Supernumerary arteries and/or early 20 arterial branching Renal arterial aneurysms 2 Renal vein anomalies 2 Atherosclerotic plaque at the renal arterial ostium 1 Duplicated IVC 1 Fibromuscular dysplasia 1
Polyarteritis nodosa 1 Renal arterio-venous malformation 1 Renal parenchyma 9 Autosomal dominant polycystic kidney disease 3 Renal cell carcinoma 2 Renal scarring 2 Complex renal cyst 1 Segmental renal infarction 1 Extra-renal 2 Pulmonary nodule 2 Katerina Mastrocostas (1); Christina M.
Polyarteritis nodosa (PAN) is included in the category of necrotizing vasculitis.
Polyarteritis nodosa in patients with familial Mediterranean fever (FMF): a concomitant disease or a feature of FMF.
Polyarteritis nodosa presenting as acute orchitis : a case report and review of the literature.
Hanslik et al., "Development and validation of a consensus methodology for the classification ofthe ANCA-associated vasculitides and
polyarteritis nodosa for epidemiological studies," Annals of the Rheumatic Diseases, vol.
Extrahepatic manifestations may include urticarial and maculopapular rash, acute kidney injury, autoimmune hemolytic anemia, aplastic anemia, acute pancreatitis, mononeuritis, reactive arthritis, Guillain-Barre syndrome and pleural or pericardial effusion, glomerulonephritis,
polyarteritis nodosa, cryoglobulinemia, and thrombocytopenia [4, 5].
However, a large number of experimental and clinical cases of SSHL have been identified in which SSHL is a symptom associated with other autoimmune diseases or is the primary symptom of spontaneous systemic autoimmune diseases such as autoimmune hepatitis [2], sympathetic neural hyperalgesia edema syndrome [3], Cogan's syndrome [4, 5], systemic lupus erythematosus [6, 7], multiple sclerosis [8-10], rheumatoid arthritis [11], nodular
polyarteritis [12], Crohn's disease [13], and so on.
DAH is associated with primary vasculitis (due to conditions such as microscopic
polyarteritis, Wegener's granulomatosis, and Churg-Strauss syndrome) and secondary vasculitis accompanying connective tissue diseases (such as SLE and malignant rheumatoid arthritis) [7].
Hadziyannis, "Post-infantile giant cell hepatitis associated with autoimmune hepatitis and
polyarteritis nodosa," Scandinavian Journal of Gastroenterology, vol.
Infectious Noninfectious Atypical mycobacteria Vascular Mycobacterium marinum
Polyarteritis nodosa Mycobacterium ulcerans ANCA-associated vasculitis Tuberculosis (cutaneous) Cryoglobulinemic vasculitis Leishmaniasis (cutaneous) Venous stasis Ecthyma gangrenosum Thrombophilia Anthrax (cutaneous) Antiphospholipid syndrome Syphilitic gumma Malignancy Deep fungal infections Squamous/basal cell carcinoma Sporotrichosis Cutaneous T-cell lymphoma Zygomycosis Drug-induced/toxin Aspergillosis Cutaneous lupus (hydralazine, (primary cutaneous) TNF-alpha inhibitors) Penicilliosis (HIV with Hydroxyurea CD4 < 100/[micro]L) Injection drug use with Venomous bite (brown secondary infection recluse spider)
HCL is known to be associated with systemic immunologic disorders including scleroderma, polymyositis,
polyarteritis nodosa, erythematous maculopapules, and pyoderma gangrenosum.
Lusan et al., "EULAR/PRINTO/PRES criteria for Henoch-Schoonlein purpura, childhood
polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008.
