Childhood polyarteritis nodosa: A rare presentation

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منابع مشابه

[Childhood cutaneous polyarteritis nodosa].

Cutaneous polyarteritis nodosa is an infrequent necrotizing vasculitis of small and medium-sized arteries, with a recurrent and chronic course, that can be associated with fever, arthralgia, myalgia and neuropathy without visceral involvement. We report a cutaneous polyarteritis nodosa case.

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Polyarteritis nodosa: an atypical presentation.

To cite: Andrade CA dos S, Vasconcelos A, Pinto JC. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2015-209564 DESCRIPTION Polyarteritis nodosa is a systemic necrotising vasculitis involving the small and medium arteries. Men aged between 40 and 60 years are more frequently affected and histological evidence of vasculitis in the involved organs is necessary for ...

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Unusual presentation of polyarteritis nodosa.

We describe an unusual presentation of a localized form of polyarteritis nodosa (PAN) manifested by acute onset of severe calf pain. Biopsies of the gastrocnemius muscle and fascia revealed an acute necrotizing arteritis with fasciitis. The lumens of affected vessels were occluded by thrombi. PAN localized to calf muscles is extremely rare. To our knowledge this is the first report of evidence ...

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Childhood polyarteritis nodosa: a clinical diagnosis.

A six-year old boy presented with dry gangrene of toes and fingers with hypertension with no other systemic abnormalities. He had persistently high inflammatory parameters, was diagnosed as childhood classic polyarteritis nodosa and showed improvement with immunosuppressants along with antihypertensives. Toe gangrene required amputation in view of superadded infection.

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Polyarteritis nodosa, with an unusual ocular presentation.

POLYARTERITIS nodosa (periarteritis nodosa), first described by Kussmaul and Maier (1866), is a relatively rare disease, but considerable attention has been paid to it in recent years. Duke-Elder (1962), describing the condition, wrote: "this is a disseminated disease of obscure cause characterized by necrosing obliterative lesions of small arteries and arterioles which appear nodular owing to ...

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ژورنال

عنوان ژورنال: Asian Journal of Medical Sciences

سال: 2016

ISSN: 2091-0576,2467-9100

DOI: 10.3126/ajms.v7i6.15724