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polyarteritis nodosa/edema
L'enllaç es desa al porta-retalls
Pàgina 1 des de 46 resultats
Fluctuating facial edema as a rare manifestation of cutaneous polyarteritis nodosa: case report and review of the literature
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Polyarteritis nodosa (PAN) is a necrotizing vasculitis. The clinical manifestations are determined by the location of the compromised arteries. Cutaneous PAN can present as nodular lesions similar to erythema nodosum, palpable purpura, livedo reticularis and ulceration. It often affects the lower
Polyarteritis Nodosa and Eosinophilic Granulomatosis With Polyangiitis Presenting as Distal Extremity Muscular Edema and Pain
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Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) as the first manifestation of periarteritis nodosa. Report of a case.
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[Backache, headache, pyrexia, systemic edema and numbness of extremities (serum reactions and serum protein freactionation): (periarteritis nodosa)].
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Polyarteritis nodosa and deafness. A human temporal bone study.
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Temporal bone changes were described in a 66 year old woman with polyarteritis nodosa who became deaf 7 months before death. Polyarteritis nodosa of the left internal auditory artery was demonstrated with fibrosis and bone formation involving the cochlea and vestibular system. Endolymphatic hydrops
[Early neuro-ophthalmological symptoms of periarteritis nodosa. A case report (author's transl)].
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A report is given on a 47-year-old woman with periarteritis nodosa. A unilateral retinopathy with disseminated cotton-wool-spots surrounded by retinal haemorrhages and edema was observed. Fluoresceinangiography showed a multifocal constriction of the retinal capillaries. This lesion of the retinal
POEMS syndrome with renal plasmacytoma and classic polyarteritis nodosa: a case report.
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POEMS syndrome is a rare conglomeration of disorders associated with plasma cell dyscrasia. The acronym POEMS is derived from main features of the syndrome namely 'polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin lesions'. Other clinical features include presence of
Intravenous immunoglobulin therapy in vasculitic ulcers: a case of polyarteritis nodosa.
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BACKGROUND
Polyarteritis nodosa (PAN) is a systemic necrotizing medium-size-vessel vasculitis with variable clinical manifestations. Diagnosis is confirmed by histology or angiography. The mainstay of treatment is corticosteroids alone or combined with cyclophosphamide
[Reversible posterior leukoencephalopathy syndrome in two patients with microscopic polyarteritis nodosa].
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We report here two cases (72-year-old woman, 77-year-old-woman) with perinuclear anti-neutrophil antibody (P-ANCA) positive microscopic polyarteritis nodosa (mPN). Both patients presented with generalized convulsion, consciousness disturbance and severe hypertension several days after the
[Oedematous polyarthritis and myopericarditis as presenting features of periarteritis nodosa].
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Remitting symmetrical seronegative synovitis with pitting edema (RS3PE) syndrome is a rare type of seronegative polyarthritis occurring in the elderly. It can be associated to various diseases. We report a case of RS3PE syndrome associated with myopericarditis, leading to the diagnosis of
Cutaneous polyarteritis nodosa.
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The term polyarteritis nodosa (PAN) presently includes classic systemic PAN, cutaneous PAN, and microscopic PAN (microscopic polyangeiitis). Cutaneous PAN involves the deep dermis and the panniculus, with anatomopathological findings diagnostic for arteritis. The most frequent clinical manifestation
[Clinical features of the peripheral nerve involvement in necrotizing angitis--characteristics in polyarteritis nodosa and allergic granulomatous angitis].
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Thirteen patients with peripheral neuropathy caused by necrotizing vasculitis were clinico-pathologically analyzed. These patients consisted of nine classical periarteritis nodosa (PN), four allergic granulomatous angitis (Churg-Strauss syndrome, AGA). All of them were proven to have a necrotizing
Clinical features of polyarteritis nodosa in Korea.
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Polyarteritis nodosa (PAN) is a systemic vasculitis characterized by multi-organ involvement with protean manifestations. We evaluated the clinical features of PAN in Korea. Twenty-seven patients were diagnosed as PAN at Seoul National University Hospital between January 1990 and July 2003. The
Polyarteritis nodosa as a cause of sudden deafness. A human temporal bone study.
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Pathological changes in the temporal bone are described in a case of polyarteritis nodosa in a 48 year old man in whom the onset of sudden unilateral deafness and vertigo occurred seven months prior to death as one of the early manifestations of the disease. The patient had received only a seven
[Two infants with classical polyarteritis nodosa but not Kawasaki disease].
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We experienced two infants with polyarteritis nodosa (PN). The symptoms started with high fever and skin rash, which were similar to those of Kawasaki disease (KD). However, the involvement of central nervous system and lung, such as distension of large fontanel, stridor and mild disturbance of
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