Vasculitis
Mostrando 1-12 de 453 artigos, teses e dissertações.
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1. IgA vasculitis in children
Brazilian Journal of Nephrology. Publicado em: 2022
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2. Leukocytoclastic vasculitis after exposure to COVID-19 vaccine
Anais Brasileiros de Dermatologia. Publicado em: 2022
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3. Surgical Repair of a Ruptured Giant Abdominal Aortic Aneurysm in a 16-Year-Old with Takayasu’s Arteritis: Case Report and Etiological Review
Abstract Takayasu’s arteritis is a type of primary systemic vasculitis that affects medium and large arteries, including the aorta and its main branches, as well as the pulmonary and coronary arteries. Although rare in children, it is the third most common vasculitis in the pediatric population, often with delayed diagnosis due to the nonspecific presentat
International Journal of Cardiovascular Sciences. Publicado em: 2022
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4. Giant Left Anterior Descending Coronary Artery Aneurysm in a Patient with Behçet’s Disease
ABSTRACT Coronary artery involvement is quite rare in the course of Behçet’s disease. Complications secondary to coronary artery aneurysms, including rupture, dissection, and myocardial ischemia, may be fatal. In young patients without cardiovascular risk factors, systemic inflammatory vasculitis syndromes should be investigated in case of acute coronary
Brazilian Journal of Cardiovascular Surgery. Publicado em: 2022
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5. Successful Surgical Treatment of Coronary Aneurysm, Ascending Aortic Aneurysm, and Bicuspid Aorta for a Kawasaki Disease Patient
Abstract Kawasaki disease was first reported in 1967, and it was classified as an autoimmune vasculitis of the small and medium arteries. It is a self-limiting condition that occurs mostly in childhood, but it may involve complications — such as coronary artery aneurysms, myocardial ischemia, and arrhythmias — with significant morbidity and mortality tha
Brazilian Journal of Cardiovascular Surgery. Publicado em: 2022
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6. Serum Syndecan-1 levels in patients with immunoglobulin A vasculitis in children
Abstract Objective The aim of this study was to evaluate the serum Syndecan-1 (SDC-1) levels in patients with immunoglobulin-A vasculitis (IgAV) in children and its relation with gastrointestinal involvements. Methods Sixty-eight children with IgAV and 48 healthy children were enrolled in this cross-sectional study. Clinical and related laboratory data wer
Jornal de Pediatria. Publicado em: 2022
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7. Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature
Resumo A glomerulonefrite rapidamente progressiva é uma emergência médica, com mortalidade em torno de 20%. É caracterizada por glomerulonefrite com crescentes e perda progressiva da função renal, hematúria e proteinúria. Sua classificação é dada pela detecção na imunofluorescência de anticorpos anti-membrana basal glomerular (Anti-MBG), imunoc
Brazilian Journal of Nephrology. Publicado em: 2022
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8. Renal biopsy in children with IgA vasculitis
Resumo Introdução A nefrite da púrpura de Henoch-Schönlein (NPHS) é definida como púrpura de Henoch-Schönlein com envolvimento renal, incluindo hematúria e/ou proteinúria. O objetivo deste estudo foi avaliar os dados de pacientes com NPHS que foram submetidos à biópsia renal e comparar os principais parâmetros clínicos e laboratoriais que podem
Brazilian Journal of Nephrology. Publicado em: 2022
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9. Lymphocytic thrombophilic arteritis with lower-limb ulcers
Abstract Lymphocytic thrombophilic arteritis is a recently described entity, histopathologically characterized by lymphocytic vasculitis that affects the arterioles of the dermo-hypodermic junction, associated with deposition of fibrin and a luminal fibrin ring. A 49-year-old female patient presented with achromic maculae and a well-defined ulcer on the medi
An. Bras. Dermatol.. Publicado em: 2021-06
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10. Case for diagnosis. Cutaneous small vessel vasculitis (anti-proteinase 3 positive), fever, hemoptysis, and lung cavitation in an adult,
Abstract Small vessel vasculitis with anti-proteinase antibodies 3 is an atypical clinical presentation of tuberculosis. The authors present the case of a 47-year-old male patient, with palpable purpura and palmoplantar hemorrhagic blisters, with subsequent dissemination. He presented severe pulmonary symptoms with cavitation, fever, hemoptysis, and high lev
An. Bras. Dermatol.. Publicado em: 2021-03
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11. Scurvy: hard to remember, easy to diagnose and treat,
Abstract Small vessel vasculitis with anti-proteinase antibodies 3 is an atypical clinical presentation of tuberculosis. The authors present the case of a 47-year-old male patient, with palpable purpura and palmoplantar hemorrhagic blisters, with subsequent dissemination. He presented severe pulmonary symptoms with cavitation, fever, hemoptysis, and high lev
An. Bras. Dermatol.. Publicado em: 2021-03
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12. Association between pemphigus and systemic lupus erythematosus: a systematic review and meta-analysis,
Abstract Small vessel vasculitis with anti-proteinase antibodies 3 is an atypical clinical presentation of tuberculosis. The authors present the case of a 47-year-old male patient, with palpable purpura and palmoplantar hemorrhagic blisters, with subsequent dissemination. He presented severe pulmonary symptoms with cavitation, fever, hemoptysis, and high lev
An. Bras. Dermatol.. Publicado em: 2021-03