Granulomatosis with polyangiitis uptodate

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      This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the ...

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      Authors: David Ost, MD, MPH. Alan Fein, MD. Steven H Feinsilver, MD. Section Editor: John G Bartlett, MD. Deputy Editor: Anna R Thorner, MD. Contributor Disclosures

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      Wegener granulomatosis (MPA) Now called ‘granulomatosis with polyangiitis’ this rare vasculitis of unknown cause has a classic triad: upper respiratory tract (URT) granuloma, fleeting pulmonary shadows (nodules) and . glomerulonephritis. Without treatment it is …

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      Primary and secondary prevention of connective tissue diseases Author: Norma Prosser, Dr Mary Webb, Public Health Specialists Date: 11 June 2010

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    • [DOC File]Actiq PA Criteria - Arkansas

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      UpToDate. Pompe Disease. Accessed 9/24/19. Date Notes Pharmacist’s initials 8/7/06 T2PA approved & criteria written. JJ 10/19/11 Lumizyme added. Someone (not I) inserted references and age specifications. JJ 5/18/12 Revision hx table added JJ 9/24/19 I revised the criteria and removed Myozyme since it is no longer available. Added reference 7. JJ

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      Eosinophilic granulomatosis with polyangiitis – Eosinophilic granulomatosis with polyangiitis (EGPA, previously called Churg-Strauss syndrome) is the major vasculitis syndrome associated with eosinophilia. Patients typically present with asthma and other lung and upper airway findings; vasculitic symptoms typically develop years later.

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    • [DOCX File]Evidence Search ServiceResults of your search request

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      Background Rituximab is a monoclonal antibody indicated in Spain in adults with non-Hodgkin's lymphoma, chronic lymphatic leukaemia, rheumatoid arthritis and granulomatosis with polyangiitis and microscopic polyangiitis.

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    • [DOC File]GHID DE TRATAMENT AL VASCULITELOR PRIMARE SISTEMICE

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      Mycophenolate mofetil for maintenance therapy of Wegener’s granulomatosis andmicroscopic polyangiitis: a pilot study in 11 patients with renal involvement. J Am Soc Nephrol 1999;10:1965–71. Zaja F, De Vita S, Mazzaro C, Sacco S, Damiani D, De Marchi G, et al. Efficacy and safety of rituximab in type II mixed cryoglobulinemia.

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      CURRICULUM VITAE: DANIEL J. WALLACE, M.D., F.A.C.P., M.A.C.R. Up to date as of February 19, 2019. Personal: Address: 8750 Wilshire Blvd, Suite 350 Beverly Hills, CA ...

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      A 53 year old man with Wegener’s Granulomatosis treated with pulsed intravenous cyclophosphamide two years ago was seen in clinic. Following treatment he became ANCA negative and had been maintained initially on steroid and azathioprine and subsequently on azathrioprine 75mg alone.

      microscopic polyangiitis uptodate


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