– Granulomatoses systémiques pseudosarcoïdosiques d’étiologie Non- tuberculous systemic granulomatosis mimicking sarcoidosis but related to a. – Granulomatoses systémiques. Mise en perspective – EM|consulte. Keywords: Systemic granulomatosis, Tuberculosis, Sarcoidosis, Diagnosis. Request PDF on ResearchGate | Les granulomatoses systémiques d’origine infectieuse | Purpose: Granulomatous diseases are defined by specific histological.

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If you originally registered with a username please use that to sign in. Pneumocystis carinii pneumonia in the course of connective tissue disease: Mean age at onset is usually 40 to 60 years old.

Close mobile search navigation Article navigation. Plasma exchange in focal necrotizing glomerulonephritis without anti-GBM antibodies.

The involved organs were the liver Don’t already have an Oxford Academic account? The precise place of new biologics, such as rituximab, needs to be further defined. It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide.

Colle aH. Efficacy and safety of rituximab in type II mixed cryoglobulinemia. Polyarteritis nodosa and Churg-Strauss angiitis: Non-tuberculous systemic granulomatosis mimicking sarcoidosis but related to a specific aetiology.

The average age at the beginning of the symptoms was Purchase Subscription prices and ordering Short-term Access To purchase short term access, please sign in to your Oxford Academic account above. Disease assessment and management of the vasculitides.


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John Libbey Eurotext – Médecine thérapeutique – Traitement des vascularites nécrosantes systémiques

Systemic vasculitis in patients with hepatitis C. Univariable analyses identified factors associated with remission failure and relapse, and Cox models retained independent predictors of relapse. Oxford University Press is a department of the University of Oxford. Access to the text HTML. This article is also available for rental through DeepDyve.

At remission, protocolized maintenance RTX infusions were given every 6 months for 18 months. Your comment will be reviewed and published at the journal’s discretion. Predictive factors and biomarkers for the 2-year outcome of uveitis in juvenile idiopathic arthritis: A prospective study with long-term observation of 41 patients.

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Clinical study and long-term follow-up of 96 patients. Treatment of polyarteritis nodosa and Churg-Strauss syndrome. Journal page Archives Contents list. Systemic granulomatosis, Tuberculosis, Sarcoidosis, Diagnosis Outline.

Thank you for submitting a comment on this article. Mise en perspective T. Their prevalences range from 24 to cases per million inhabitants.

Long-term followup of polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss syndrome: Most common and suggestive features of Wegener’s granulomatosis are upper sinusitis, crusting rhinitis, saddle nose deformity, systemiqies media and lower excavated lung nodules, alveolar hemorrhage respiratory tract, and kidney involvements.

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Contact Help Who are we? Prognostic factors in polyarteritis nodosa syshemiques Churg-Strauss syndrome. Rituximab for induction and maintenance therapy of granulomatosis with polyangiitis: Systemic granulomatosis, Tuberculosis, Sarcoidosis, Diagnosis.


Antiviral treatment and outcome in patients with hepatitis C virus systemic vasculitis.

[Wegener’s granulomatosis and microscopic polyangiitis].

Citing articles via Google Scholar. You can move this window by clicking on the headline. Therapy relies on the combination of corticosteroids and pulse intravenous cyclophosphamide, which can be switched, as soon as remission is achieved, to azathioprine or methotrexate, for a total duration of treatment of grannulomatoses least 18 months. Outline Masquer le plan. Personal information regarding our website’s visitors, including their identity, is confidential.

[Wegener’s granulomatosis and microscopic polyangiitis].

Indications of plasma exchanges, meta-analysis of 2 randomized studies on patients, 32 with syystemiques. Autoantibodies in neuropsychiatric lupus: Kidney transplantation for treatment of end-stage kidney disease after haematopoietic stem cell transplantation: The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.

ANCA anti-idiotype antibodies and the treatment of systemic vasculitis with intravenous immunoglobulin.

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