– 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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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 at least 18 months. Efficacy and safety of rituximab in type II mixed cryoglobulinemia.

[Wegener’s granulomatosis and microscopic polyangiitis].

Prognostic factors in polyarteritis nodosa and Churg-Strauss syndrome. Systemic vasculitis in patients with hepatitis C.

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Serious infection and serious adverse event rates were 4. Personal information regarding our website’s visitors, including their identity, is confidential. The precise place of new biologics, such as rituximab, needs to be further defined.

Antiviral treatment and outcome in patients with hepatitis C virus systemic vasculitis. Systemique per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data.


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Pneumocystis carinii pneumonia in the course of connective tissue disease: Non-tuberculous systemic granulomatosis mimicking sarcoidosis but related to a specific aetiology. The granuloma were detected mainly in the liver Most common and suggestive features of Wegener’s granulomatosis are upper sinusitis, crusting rhinitis, saddle nose deformity, otitis media and lower excavated lung nodules, alveolar hemorrhage respiratory tract, and kidney involvements.

Most users should sign in with their email address. At remission, protocolized maintenance RTX infusions were given every 6 months for 18 months. The median diagnostic delay was one year. Systemic granulomatosis, Tuberculosis, Sarcoidosis, Diagnosis.

Access to the PDF text. Top of the page – Article Outline. Indications of plasma exchanges, meta-analysis of 2 randomized studies on patients, 32 with glomerulonephritis. Sign In or Create an Account.

Granulomatoses systémiques. Mise en perspective – EM|consulte

Rituximab for induction and maintenance therapy of systemiquea with polyangiitis: Long-term followup of polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss syndrome: Latest Most Read Most Cited Predictors of fatigue and severe fatigue in a large international cohort of granulo,atoses with systemic lupus erythematosus and a systematic review of the literature. RTX induction and low-dose preemptive maintenance can effectively and safely induce sustained remission in GPA in a real-life setting.


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This article is also available for rental through DeepDyve. Contact Help Who are we? You can move this window by clicking on the headline. Purchase Subscription granulmoatoses and ordering Short-term Access To purchase short term access, please sign in to your Oxford Academic account above. Clinical study and long-term follow-up of 96 patients. Sixty-seven cases were included in the study.

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Debourdeau aD. General symptoms were present in Methotrexate achieves major cDAPSA response, and improvement in dactylitis and functional status in psoriatic arthritis.

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Mean age at onset is usually 40 to 60 years old.