Antiphospholipid
Mostrando 1-12 de 150 artigos, teses e dissertações.
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1. Catastrophic antiphospholipid syndrome post-Epstein-Barr virus infection: a case report
Hematology, Transfusion and Cell Therapy. Publicado em: 2022
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2. Non-criteria Antiphospholipid Antibodies: a narrative review
RESUMO A classificação de Sapporo revisada para a síndrome antifosfolipídica definida de 2006 incluiu como critérios laboratoriais aqueles testes para anticorpos antifosfolípides cuja acurácia era considerada satisfatória de acordo com a evidência então disponível. Porém, na prática, a sensibilidade e especificidade desses anticorpos antifosfol�
Rev. Assoc. Med. Bras.. Publicado em: 2020-11
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3. Evans syndrome associated with antiphospholipid antibodies in a patient with SARS-COV-2 infection
The chemists from Latin-America need to do more to achieve equality in the scientific world and gain greater recognition by the broader chemical community. For this, we should rethink our strategy to fight for a more inclusive science, not only internationally but also within our region. Raise your hands and take actions to support this movement.
Hematol., Transfus. Cell Ther.. Publicado em: 2020-10
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4. Successful treatment of catastrophic antiphospholipid syndrome with therapeutic plasma exchange: a case report
Resumo A construção das identidades negras no Brasil é marcada por uma série de lutas que influenciaram diretamente os avanços institucionais recentes em relação à temática, além de contribuírem para a desconstrução do mito da democracia racial. O objetivo deste artigo é compreender e analisar como se apresentam elementos relacionados às rela�
Hematol., Transfus. Cell Ther.. Publicado em: 2020-09
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5. Anetoderma: an alert for antiphospholipid antibody syndrome,
Abstract Erythroderma as the first manifestation of a solid organ malignancy is rare. The underlying cancer is a challenging condition to diagnose. There are a few cases of erythroderma in cancer patients reported in the literature. We here describe the case of a 70-year-old man who presented with asthenia, weight loss, dry cough and total body erythema with
An. Bras. Dermatol.. Publicado em: 2020-02
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6. Epidemiological, clinical and immune factors that influence the persistence of antiphospholipid antibodies in leprosy
Abstract Introduction: Antiphospholipid antibodies (aPL) are described in individuals with leprosy without the clinical features of antiphospholipid antibody syndrome (APS), a condition involving thromboembolic phenomena. We have described the persistence of these antibodies for over 5 years in patients with leprosy after specific treatment. Objectives: To
Adv. rheumatol.. Publicado em: 09/12/2019
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7. Risk factors and role of low molecular weight heparin in obstetric complications among women with inherited thrombophilia - a cohort study
ABSTRACT Introduction: Although there is a vast literature regarding the association between inherited thrombophilia, obstetric complications and the effect of low molecular weight heparin (LMWH), these are controversial and we have not found publications related to additional risk factors other than thrombophilia.Our objectives were to assess the prevalenc
Hematol., Transfus. Cell Ther.. Publicado em: 25/11/2019
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8. Antiphospholipid Antibody Syndrome and Infertility
Resumo A Síndrome do anticorpo antifosfolípide (SAF) é uma doença sistêmica, autoimune e prótrombótica caracterizada por anticorpos antifosfolípides, trombose, aborto recorrente, complicações durante a gestação, e, ocasionalmente, trombocitopenia. O objetivo do presente estudo foi revisar a fisiopatologia da SAF e sua associação com a infertili
Rev. Bras. Ginecol. Obstet.. Publicado em: 07/11/2019
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9. Primary antiphospholipid syndrome in a hemodialysis patient with recurrent thrombosis of arteriovenous fistulas
RESUMO Introdução: A síndrome antifosfolipídica é uma doença autoimune sistêmica definida por morbidade vascular e/ou obstétrica, recorrente, que acomete pacientes com anticorpos antifosfolípides persistentes. Apresentação do caso: Uma paciente em hemodiálise com síndrome antifosfolípide primária apresentou trombose recorrente do acesso vas
J. Bras. Nefrol.. Publicado em: 29/07/2019
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10. Panniculitis in childhood-onset systemic lupus erythematosus: a multicentric cohort study
Abstract Objective: To evaluate prevalence, clinical manifestations, laboratory abnormalities, treatment and outcome in a multicenter cohort of childhood-onset systemic lupus erythematosus (cSLE) patients with and without panniculitis. Methods: Panniculitis was diagnosed due to painful subcutaneous nodules and/or plaques in deep dermis/subcutaneous tissues
Adv. rheumatol.. Publicado em: 29/07/2019
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11. Antiphospholipid syndrome and neurofibromatosis type I: a coincidence or new association?
RESUMO | Inúmeros estudos têm relatado anomalias vasculares estruturais e isquemia associada com à neurofibromatose tipo 1 que, acredita-se, resultam da disfunção da neurofibromina, a proteína tipo 1 da neurofibromatose. Casos documentados de síndrome antifosfolípide associada que atendem aos critérios diagnósticos aceitos são excepcionalmente rar
Arq. Bras. Oftalmol.. Publicado em: 2019-03
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12. Anti-phospholipid syndrome in seven leprosy patients with thrombotic events on corticosteroid and/or thalidomide regimen: insights on genetic and laboratory profiles
Abstract INTRODUCTION Corticosteroids and/or thalidomides have been associated with thromboembolism events (TBE) in multibacillary (MB) leprosy. This report aimed to determine genetic and laboratory profiles associated with leprosy and TBE. METHODS Antiphospholipid antibodies (aPL), coagulation-related exams, prothrombin and Leiden’s factor V mutations
Rev. Soc. Bras. Med. Trop.. Publicado em: 2018-02