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systemic vasculitis/πυρετός
Ο σύνδεσμος αποθηκεύεται στο πρόχειρο
Σελίδα 1 από 303 Αποτελέσματα
Standardised work-up programme for fever of unknown origin and contribution of magnetic resonance imaging for the diagnosis of hidden systemic vasculitis.
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Σύνδεση εγγραφή
BACKGROUND
Fever of unknown origin (FUO) is a diagnostic challenge. Rheumatologists are often in charge of patients with FUO because the vasculitides, especially, are potential and common causes of FUO.
OBJECTIVE
To evaluate the value of a standardised investigation to identify the cause of
[Systemic vasculitis as a cause of fever of unknown origin].
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Σύνδεση εγγραφή
A prospective clinical study (1974-1988) was carried out in 33 patients with several types of systemic vasculitis (SV) presenting as fever of unknown origin (FUO) according to the 1961 Petersdorf and Beeson's criteria. Histological confirmation, either from biopsy or necropsy, was available in all
Systemic vasculitis with prolonged pyrexia, recurrent facial urticaria, skin nodules, pleural effusions and venous thrombosis: an unusual presentation of an uncommon disease.
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Σύνδεση εγγραφή
Classically presenting with multiple or single peripheral cytopenias of variable severity, the myelodysplastic syndromes may occasionally present with bizarre manifestations that confuse the clinical picture and result in significant delays in making the correct diagnosis. We describe the case of an
Polyarteritis nodosa in case of familial Mediterranean fever.
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Σύνδεση εγγραφή
Gökçe İ, Altuntaş Ü, Filinte D, Alpay H. Polyarteritis nodosa in case of familial Mediterranean fever. Turk J Pediatr 2018; 60: 326-330. Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever accompanied by peritonitis,
A retrospective study of radiolabeled granulocyte kinetics in patients with systemic vasculitis.
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Σύνδεση εγγραφή
Patients with systemic vasculitis, including Wegener's granulomatosis (WG) and microscopic polyarteritis (MP), may undergo white cell scanning for the investigation of infective complications and/or occult fever. In a retrospective study of 12 patients with systemic vasculitis (six each of WG and
[Anti-endothelial cell antibodies in systemic vasculitis: detection and correlation with disease activity].
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Σύνδεση εγγραφή
OBJECTIVE
To investigate the prevalence of anti-endothelial cell antibodies (AECA) in systemic vasculitis and to assess the correlation between AECA and disease activity, and try to discuss the classification of AECA.
METHODS
Cyto-ELISA with EA.hy926 and HMEC-1, two immortalized cell lines, as
Fulminant systemic vasculitis in systemic lupus erythematosus. Case report and review of the literature.
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Σύνδεση εγγραφή
Vasculitis in systemic lupus erythematosus (SLE) has a broad spectrum of clinical manifestations from cutaneous to visceral involvement and its prognosis ranges from mild to life-threatening. We report the case of a previously healthy 17-year-old woman with eight months' history of arthralgias and
[Systemic necrotizing vasculitis in autopsy].
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Σύνδεση εγγραφή
OBJECTIVE
To analyze the characteristics of systemic necrotizing vasculitis observed in necropsy emphasizing the non-diagnosed cases until necropsy and to identify the reasons of clinical confusion.
METHODS
Necropsies of adult patients performed in Hospital General La Paz, Madrid, from 1966 to 1977
Prognostic factors in systemic necrotizing vasculitis of the polyarteritis nodosa group--a review of 45 cases.
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Σύνδεση εγγραφή
OBJECTIVE
To evaluate the prognostic importance for mortality of age, fever, hypertension, and involvement of renal, cardiac, neural, pulmonary, gastrointestinal and cutaneous systems as well as elevated transaminases, thrombocytosis, leukocytosis, anemia, smoking status, comorbid diseases and
Systemic vasculitis with gastrointestinal involvement in an HIV-infected adult.
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Σύνδεση εγγραφή
Several types of human immunodeficiency virus (HIV)-associated vasculitides, including polyarteritis nodosa-like syndromes have been reported in patients with HIV infection. The pathogenic mechanism is thought to be related to either circulating immune complexes or direct endothelial involvement by
Infective endocarditis due to Bartonella bacilliformis associated with systemic vasculitis: a case report.
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Σύνδεση εγγραφή
Infective endocarditis due to Bartonella bacilliformis is rare. A 64-year-old woman, without previous heart disease, presented with 6 weeks of fever, myalgias, and arthralgias. A systolic murmur was heard on the tricuspid area upon examination, and an echocardiogram showed endocardial lesions in the
Cogan's syndrome: organ-specific autoimmune disease or systemic vasculitis? A report of two cases and review of the literature.
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Σύνδεση εγγραφή
Cogan's syndrome is a rare disorder of unknown origin characterized by inflammatory eye disease and vestibuloauditory symptoms. Typically, young adults suffer from interstitial keratitis and sudden onset of tinnitus and hearing loss. Few cases (around 150) have been published and thus it is
Impaired function of endothelial progenitor cells in children with primary systemic vasculitis.
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Σύνδεση εγγραφή
BACKGROUND
Previously, we demonstrated that children with active systemic vasculitis (SV) have higher circulating CD34 + CD133 + KDR+ endothelial progenitor cells (EPC); the function of these EPCs, and their relationship with disease activity in vasculitis remains largely unexplored. We hypothesized
[The 451(th) case: intermittent rash, fever and headache].
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Σύνδεση εγγραφή
A 29-year-old woman was admitted to the Department of Rheumatology, Peking Union Medical College Hospital due to intermittent rashes, fever and headache. Palpable purpura were symmetrically distributed on the extremities and trunk. Other manifestations included headache with nausea and vomiting.
Systemic vasculitis with bilateral perirenal haemorrhage in chronic myelomonocytic leukaemia.
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Σύνδεση εγγραφή
The cases of two patients with chronic myelomonocytic leukaemia associated with periarteritis nodosa-like, antineutrophil cytoplasmic antibody negative, systemic vasculitis, are reported. A 61 year old man was admitted with fever, diffuse myalgia, and abdominal pain. Blood and bone marrow
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