Chronic polyarthritis as the first manifestation of childhood systemic polyarteritis nodosa

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Chronic polyarthritis as the first manifestation of childhood systemic polyarteritis nodosa

Arthritis has been reported as an acute pattern, generally evanescent with oligoarthritis, mostly affecting knees and ankles in childhood systemic polyarteritis nodosa. However, chronic polyarthritis with morning stiffness mimicking juvenile idiopathic arthritis has not been reported. We describe the case of a 4-year old girl who had additive and chronic polyarthritis with edema, tenderness, pa...

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Systemic fibromuscular dysplasia masquerading as polyarteritis nodosa.

The diagnosis of systemic diseases, such as vasculitis, may be difficult because of an uncharacteristic clinical presentation or the inability to obtain histopathological confirmation. Classification criteria for the systemic vasculitides have been composed as a guide for the diagnostic process. If polyarteritis nodosa (PAN) is strongly suspected histological confirmation is not mandatory for t...

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[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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Raynaud's phenomenon as initial manifestation of cutaneous polyarteritis nodosa.

The case of a 45 year old man with cutaneous polyarteritis nodosa and Raynaud's phenomenon as initial manifestation of the disease is reported. Although peripheral vascular disease is a well characterised extracutaneous manifestation of cutaneous polyarteritis nodosa, to our knowledge this is the first reported case in which Raynaud's phenomenon was the initial and sole manifestation of the dis...

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A previously healthy 89-year-old man was admitted to our hospital with right upper quadrant pain and mild fever. A diagnosis of cholangitis was suspected based on the patient's physical findings and imaging features. Although he received treatment typical for cholangitis, he suddenly died of shock for unknown reasons two months after disease onset. An autopsy revealed a ruptured hepatic artery ...

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ژورنال

عنوان ژورنال: Einstein (São Paulo)

سال: 2017

ISSN: 1679-4508

DOI: 10.1590/s1679-45082017rc3783