Prognosis for limited systemic scleroderma

    • [DOC File]Six chapters 2014 - University of Jordan

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      Limited scleroderma: long Hx raynauds, scleroderma distal to knees and elbows, anywhere else = diffuse, lung disease pulmonary HTN + digital ischaemia > ILD, cardiac and renal disease rare, Antibodies = centromere, nucleolar and speckled, if centromere + decreased risk of ILD + pulm HTN

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    • [DOC File]| Universitatea de Stat de Medicină și Farmacie "Nicolae ...

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      Individuals with morphea or limited scleroderma have a relatively positive outlook. Those with diffuse systemic scleroderma have a negative prognosis, and although more females are affected, the disease kills more men. Following diagnosis, two-thirds of patients live at least 11 years.

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    • [DOC File]National PBM Monograph Template Rev20091005

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      Prognosis. 25-50% re-bleed in the next 5 years – mortality rate for a re-bleed is 30%; however, without re-bleeding, mortality rate is 3%. Factors associated with mortality – underlying renal, liver, neoplastic, CNS, or lung disease, and physical findings consistent with cardiorespiratory or hemodynamic compromise, or liver failure.

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    • Systemic scleroderma - Wikipedia

      There is a need for new systemic sclerosis subset criteria.A content analytic approach. Sindhu R Johnson, Medha L Soowamber, Jaap Fransen, Dinesh Khanna, Frank van ...

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    • [DOCX File]Background - Dis Lair

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      Potential off-label uses of nilotinib include: treatment of CML in the blastic phase that is resistant or intolerant to imatinib, Philadelphia chromosome-positive, relapsed/refractory Acute lymphoid leukemia (ALL), systemic mast cell disease, Gastrointestinal Stromal Tumors (GIST), systemic sclerosis, scleroderma and other fibrotic conditions.

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    • [DOCX File]Gout and Other Crystal Arthopathies

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      ii. Scleroderma (a) Autoimmune connective tissue disease causing fibrotic changes to the skin, blood vessels, muscles, and internal organs (b) Can be either localized or systemic (1) One third of the estimated 300,000 cases in the United States are systemic. (2) Children are more likely to have localized, while adults tend to have systemic

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    • [DOC File]Emergency Care and Transportation of the Sick and Injured ...

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      Progressive systemic sclerosis (scleroderma) including the diffuse and limited (formerly called. CREST syndrome) Systemic lupus erythematosus. Mixed connective-tissue disease (and other overlap syndromes) Dermatomyositis and polymyositis. Rheumatoid arthritis. Sjögren syndrome. Vasculitis. Primary pulmonary hypertension. Infectious syndromes

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    • [DOC File]General Surgery—GI Bleeds and Intestinal Obstruction

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      Remember that disease of the joints may be a secondary manifestation of a systemic disease. Examples of conditions that you should know a short paragraph for are: Rheumatoid Arthritis, Systemic Lupus Erythematosus, Scleroderma, Chronic Renal Failure, Ankylosing Spondylitis, Osteoporosis, Paget’s disease & Endocrine Diseases.

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    • [DOCX File]www.research.manchester.ac.uk

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      Prognosis with treatment is good in early and light to moderate infections if reinfection does not occur. With heavy infestations, and extensive involvement the outlook is poor even with treatment. Death commonly results from incurrent disease, often within a few years after the infestation.

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    • [DOC File]M29-1, Part 5, S

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      Skin limited Systemic Scleroderma. Visceral Systemic Scleroderma . Systemic Scleroderma „sine scleroderma” Enumerate the minor criterias for diagnosis of Systemic Scleroderma: Sclerodactyly. Bilateral basilar pulmonary fibrosis . Tendon-synovia affection. Digital ulcerations and/or scars on distal phalanges . Fever. Specify the anti ...

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