Revista Brasileira de Reumatologia, 2007 É apresentado um caso inusitado de poliarterite nodosa em uma mulher de 57 anos, que se manifestou por aumento progressivo das panturrilhas, com discreta manifestação sintomática local.
Mauro Goldfarb +2 more
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Polyarteritis Nodosa: Clinical Cases in Boys 12 and 9 Years Old
Кубанский научный медицинский вестник, 2023 Background. Polyarteritis nodosa is an acute, subacute or chronic immune complex disease associated with peripheral and visceral artery involvement, predominantly of middle and small sizes, development of destructive-proliferative arteritis and ...
A. V. Burlutskaya +5 more
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A case of polyarteritis nodosa limited to the right calf muscles, fascia, and skin: a case report [PDF]
, 2011 Introduction Limited polyarteritis nodosa is a rare benign disease that usually responds well to systemic corticosteroid treatment. We report a case limited to calf muscles, fascia, and skin treated with local corticosteroid therapy directed to the ...
Saad Ahmed +4 more
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Leg muscle involvement in polyarteritis nodosa (limited form)—A rare case report
Radiology Case Reports, 2023 Polyarteritis nodosa is a necrotizing arteritis involving small and medium vessels. Polyarteritis nodosa can have variable presentations depending upon the organ involved.
Rishabh Pratap, MBBS, Gaurav Raj, MD
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Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
Rheumatology, 2019 Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective tissue diseases, infectious diseases or malignancies.
Izabela Dybowska-Gołota +2 more
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PR3-ANCA in Wegener's granulomatosis prime human mononuclear cells for enhanced activation via TLRs and NOD1/2 [PDF]
, 2009 Background Anti-neutrophil cytoplasmic antibodies (ANCA) is autoantibodies characteristic of vasculitis diseases. A connection between ANCA and Wegener's granulomatosis was well established. The interaction of both ANCA phenotypes (PR3-ANCA and MPO-ANCA)
Iwashiro Atsushi +3 more
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Cutaneous polyarteritis nodosa causing refractory skin deformation and pigmentation as sequel [PDF]
Anais Brasileiros de Dermatologia, 2017 : A 39-year-old woman presented with prominent and painful livedo reticularis lesions spreading on her upper and lower extremities. Histopathologically, the small-to medium-sized arteries in the deep dermis and subcutis showed necrotizing vasculitis with
Karin Okada +3 more
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Eosinophilic granulomatosis with polyangiitis (EGPA) and PRES: a case-based review of literature in ANCA-associated vasculitides [PDF]
, 2015 Eosinophilic granulomatosis with polyangiitis (EGPA) is a small-sized vessel systemic necrotizing vasculitis and belongs to the family of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides.
Barilaro, Giuseppe +3 more
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Medical geography and its contribution to the aetiology of rare systemic connective tissue diseases : a thesis presented in partial fulfilment of the requirements for the degree of Master of Arts in Geography at Massey University [PDF]
, 1975 This thesis is in two interrelated parts. Part One traced the historical development of medical geography since the idea of applying a geographical perspective to medical problems was first mooted in 4 B.C.
Borman, Graham Barry
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