Retroperitoneal Fibrosis and Polyarteritis Nodosa
نویسندگان
چکیده
منابع مشابه
Polyarteritis Nodosa
POLYARTERITIs NODosA, as its niame implies, is ain inflammatory lesion involving the -whole three coats of the arterial system in a noclal manner. The causation of this is unknown, but its peculiar affinity for wi(despread involvement of the smaller arteries results in a multiplicity of clinical signs and symptoms, and leads to confusion and difficulty in diagnosis. The more severely affected o...
متن کاملPolyarteritis Nodosa
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, the definition or criteria of systemic vas...
متن کاملPolyarteritis nodosa.
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. Because of the striking pattern of his fevers, he was diagnosed for man...
متن کاملPolyarteritis nodosa following angioplasty.
1 Graf M W, Uhr J W. Regulation of antibody formation by serum antibody. I. Removal of specific antibody by means of immunoadsorption. Exp Med 1969; 130: 1175-86. 2 Bystryn J C, Graf M W, Uhr J W. Regulation of antibody formation by serum antibody. II. Removal of specific antibody by means of exchange transfusion. Exp Med 1970; 132: 1279-87. 3 Verrier Jones J, Robinson M F, Parciany R K, Layfer...
متن کاملCutaneous polyarteritis nodosa*
Polyarteritis nodosa is a rare vasculitis in children characterized by necrotizing inflammation in small and medium size arteries. It is classified into systemic and cutaneous PAN according to the presence of systemic symptoms or visceral involvement. We describe the case of a 14-year-old girl with cutaneous Polyarteritis nodosa with an atypical clinical presentation.
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 1980
ISSN: 0141-0768,1758-1095
DOI: 10.1177/014107688007300521