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Polyarteritis Nodosa

2016
Polyarteritis nodosa (PAN) is a rare vasculitis affecting middle-sized arteries. Its annual incidence in Europe is estimated to range between 0 and 1.6 cases per million, while the prevalence is about 31 cases per million. The frequency of hepatitis B virus (HBV)-related PAN has declined in developed countries since vaccination against HBV has been ...
Pipitone N., Salvarani C.
openaire   +2 more sources

Cutaneous Polyarteritis Nodosa

Seminars in Cutaneous Medicine and Surgery, 2007
The term polyarteritis nodosa (PAN) presently includes classic systemic PAN, cutaneous PAN, and microscopic PAN (microscopic polyangeiitis). Cutaneous PAN involves the deep dermis and the panniculus, with anatomopathological findings diagnostic for arteritis.
José L, Díaz-Pérez   +3 more
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Polyarteritis nodosa revisited

Current Rheumatology Reports, 2005
Polyarteritis nodosa (PAN), the prototype of systemic vasculitis, is a rare condition characterized by necrotizing inflammation of medium-sized or small arteries without glomerulonephritis or vasculitis in arterioles, capillaries, or venules. Signs and symptoms of this disease are primarily attributable to diffuse vascular inflammation and ischemia of ...
Inés, Colmegna   +1 more
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Muscular Polyarteritis Nodosa

JCR: Journal of Clinical Rheumatology, 2012
We present an unusual case of a 26-year-old man with muscular polyarteritis nodosa (PAN) with severe calf pain and gait disturbance. Magnetic resonance imaging of the lower limbs demonstrated highly increased signal intensity in both soleus muscles and the lateral head of the left gastrocnemius muscle.
Seung Nam, Yang   +5 more
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Cutaneous Polyarteritis Nodosa Sine Nodosa

Journal of Cutaneous Medicine and Surgery, 2014
Background and Objective: Cutaneous polyarteritis nodosa, a form of vasculitis affecting the small to medium sized arteries, most commonly presents as tender subcutaneous nodules over the lower legs and feet. Other features include livedo reticularis, skin ulcers and tender indurated plaques.
Erica, Merman   +4 more
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Polyarteritis Nodosa

JAMA, 2002
Polyarteritis nodosa (PAN) is regarded rightly as the grandfather of the vasculitides. In this Grand Rounds, the case of a 30-year-old man with a 12-year illness is described. The patient presented with daily fevers, tachycardia, and cutaneous ulcers on his distal extremities. He eventually developed mononeuritis multiplex.
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CUTANEOUS POLYARTERITIS NODOSA

British Journal of Dermatology, 1972
Summary.— The case histories of 102 consecutive patients suffering from polyarteritis nodosa were reviewed. The 17 patients with skin lesions were personally examined and investigated. Thirteen were found to have polyarteritis affecting the skin. In one of these cutaneous involvement occurred only 4 days before death and 5 weeks after the onset of the ...
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Polyarteritis nodosa.

Journal of insurance medicine (New York, N.Y.), 2006
Polyarteritis nodosa is a systemic necrotizing vasculitis of small and medium-sized arteries affecting multiple organ systems. Typical findings are illustrated.
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Bleeding polyarteritis nodosa

International Journal of Rheumatic Diseases, 2023
Rui Wu, Jiarui Hu, Huanyue Hai, Jing Zhu
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[Polyarteritis nodosa].

Nihon rinsho. Japanese journal of clinical medicine, 1999
Polyarteritis nodosa (PAN) is the systemic necrotizing vasculitis on small and median muscular vessels. Recent studies reveal that PAN consists of classical PAN and microscopic polyangitis (MPA). MPO-ANCA, which is one of anti-neutrophil cytoplasmic antibody (ANCA), is involved in the pathogenesis of MPA. In future, by the progress of research of ANCA,
M, Murakami, S, Ozaki, K, Nakao
openaire   +1 more source

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