relapsing polychondritis
policondritis recidivante
polychondric oor Spaans
polychondric
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policóndrico
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Relapsing polychondritis: An study of 19 cases in Colombia
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It appears to have limited effect in relapsing polychondritis, as it may only be useful for the treatment of chondritis and mild skin symptoms.
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Rheumatic disorders, in particular rheumatoid arthritis, polychondritis, Bechterew's disease, fibromyalgia and/or lupus erythematosus
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At the end, there is a list of some rheumatic manifestations of neoplastic disorders and special emphasis is placed on relapsing polychondritis as a possible para-neoplastic manifestation, highlighting that there are very few associations reported in the national and international literature between relapsing polychondritis and malignant lymphoma.
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Peripheral ulcerative keratitis is a serious corneal ulceration; it often occurs with autoimmune connective tissue diseases that are active, long-standing, or both, such as RA, granulomatosis with polyangiitis (formerly called Wegener granulomatosis), and relapsing polychondritis.
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Introduction to Autoimmune Rheumatic Relapsing polychondritis is an episodic, inflammatory, and destructive disorder involving primarily cartilage of the ear and nose but also potentially affecting the eyes, tracheobronchial tree, heart valves, kidneys, joints, skin, and blood vessels.
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People who have relapsing polychondritis are at increased risk of atherosclerosis (see Atherosclerosis) and are closely monitored by doctors.
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To analyze 11 patients with relapsing polychondritis reported by 3 hospitals in our country.
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Mayo's rheumatologists treat more than 100 types of arthritis, including common diseases such as rheumatoid arthritis and osteoarthritis, and rare diseases such as relapsing polychondritis and multicentric reticulohistiocytosis.
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Keywords: POLYCHONDRITIS, RELAPSING.
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Relapsing Polychondritis: An Analysis of 11 Patients | Reumatología Clínica (English Edition)
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We present a case of relapsing polychondritis associated to low degree lymphoplasmocytic lymphoma whose picture was punctuated by cutaneous erythema nodosum and anterior uveitis.
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Due to its typically clinical picture, as well as to the results of complementary studies, recurrent polychondritis (PR) is diagnosed, steroids and conventional treatment are prescribed for chronic respiratory failure (CRF). Despite treatment, the patient had torpid evolution.
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We present a case of relapsing polychondritis, stating clinical and therapeutic issues about a disease that is clinically diagnosed, with the typical signs and symptoms of a systemic disease, and emphasize on the need for a multidisciplinary approach of the patient suffering from an immune-mediates systemic disease.
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Relapsing polychondritis (RP) is an unusual systemic autoimmune disease, of unknown etiology and recurrent nature, that is more frequent between the third and the fourth decade of life.
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Due to its typically clinical picture, as well as to the results of complementary studies, recurrent polychondritis (PR) is diagnosed, steroids and conventional treatment are prescribed for chronic respiratory failure (
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Relapsing polychondritis: clinical presentation diagnosis and treatment
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Immunologic mechanisms play a role in the pathogenesis of relapsing polychondritis.
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Mild relapsing polychondritis of the ear can be treated with nonsteroidal anti-inflammatory drugs (NSAIDs—see see Nonopioid Analgesics: Nonsteroidal Anti-Inflammatory Drugs) or dapsone.
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Peripheral ulcerative keratitis is a serious corneal ulceration; it often occurs with autoimmune connective tissue diseases that are active, long-standing, or both, such as RA, granulomatosis with polyangiitis (formerly called Wegener granulomatosis), and relapsing polychondritis. Patients often have decreased visual acuity, photophobia, and foreign body sensation.
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Having an autoimmune condition, including Riedel thyroiditis, primary sclerosing cholangitis, retroperitoneal fibrosis, and polychondritis, limited systemic sclerosis, or having elevated IgG4 in the blood and/or autoimmune pancreatitis
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Relapsing polychondritis has been estimated to have an incidence of 3.5 per million population per year.
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Sjögren Polychondritis Eosinophilic Fasciitis Mixed connective tissue disease is a term used by some doctors to describe a disorder characterized by features of systemic lupus erythematosus, systemic sclerosis, and polymyositis.
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ERISPAN and other glucocorticoids are still the primary treatment to control symptoms and prevent severe complications, often life-threatening in patients with dermatomyositis and polymyositis, polyarteritis nodosa, relapsing polychondritis, polymyalgia rheumatica and arteritis (temporal) of the giant cells, or mixed syndrome of connective tissue disease.
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* July - August 2007 Relapsing Polychondritis: An Analysis of 11 Patients
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