Polyarteritis Nodosa Inducing Symmetric Peripheral Gangrene
نویسندگان
چکیده
منابع مشابه
Cutaneous Polyarteritis Nodosa Presented with Digital Gangrene: A Case Report
Cutaneous polyarteritis nodosa (CPAN) is an uncommon form of vasculitis involving small and medium sized arteries of unknown etiology. The disease can be differentiated from polyarteritis nodosa by its limitation to the skin and lack of progression to visceral involvement. The characteristic manifestations are subcutaneous nodule, livedo reticularis, and ulceration, mostly localized on the lowe...
متن کاملFatal polyarteritis presenting as asymmetrical peripheral gangrene.
Peripheral gangrene is one of the rarest presenting features in polyarteritis nodosa. A man with paralysed right upper and left lower limbs following poliomyelitis in infancy was admitted to hospital with supraventricular tachycardia and peripheral gangrene in the non-involved extremities. In an attempt to relieve the severe foot pain following an exacerbation of the arteritis, intermittent epi...
متن کاملPolyarteritis 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...
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ژورنال
عنوان ژورنال: Circulation
سال: 2003
ISSN: 0009-7322,1524-4539
DOI: 10.1161/01.cir.0000068032.38990.85