ACR Meeting Abstracts

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Abstracts tagged "Behcet’s syndrome"

  • Abstract Number: 1790 • 2018 ACR/ARHP Annual Meeting

    An Unmet Need for Oral Ulcer Activity in Patients with Behcet’s Disease: A Multi-National Study

    Gonca Mumcu1, Adebowale Adesanya2, Aysun Aksoy3, Joice Moraes Faria M Belem4, Natalia Borges Cardin4, Fatma Alibaz-Oner5, Tulin Ergun6, Nevsun Inanc7, Alexandre W.S. Souza8, Wafa Madanat9, Farida Fortune10 and Haner Direskeneli7, 1Department of Health Management, Marmara University, Faculty of Health Sciences, Istanbul, Turkey, 2Barts and The London, School of Medicine and Dentistry, Institute of Dentistry, Clinical and Diagnostic Oral Sciences, London, UK, London, United Kingdom, 3Rheumatology, Marmara University School of Medicine, Istanbul, Turkey, 4Rheumatology, Universidade Federal de Sao Paulo, Sao Paulo, Brazil, 5Şerifali mahallesi İbrahim Hakkı sokak. Lavella 4 sitesi. B blok, D:22 Umraniye, Şerifali mahallesi İbrahim Hakkı sokak. Lavella 4 sitesi. B blok, D:22 Umraniye, Istanbul, Turkey, 6Department of Dermatology, Faculty of Medicine, Marmara University, Istanbul, Turkey, 7Rheumatology, Marmara University, School of Medicine, Istanbul, Turkey, 8Rheumatology Division, Universidade Federal de São Paulo, Sao Paulo, Brazil, 9Jordan’s Friends of Behcet’s disease Patients Society, Medical department, Amman, Jordan, Amman, Jordan, 10Dental Institute, Barts and The London NHS Trust, London, United Kingdom

    Background/Purpose: Efficacy of current management approaches for oral ulcer treatment in routine clinical practice is insufficiently explored in Behcet’s disease (BD) patients. The aim of…
  • Abstract Number: 1811 • 2018 ACR/ARHP Annual Meeting

    Efficacy and Safety of Interferon α2a As an Add-on Treatment for Refractory Behcet’s Uveitis

    Jing Shi1, Chan Zhao2, Jiaxin Zhou3, JinJing Liu1, Fei Gao2, Xiaofeng Zeng4, Meifen Zhang2 and Wenjie Zheng1, 1Rheumatology, Peking Union Medical College Hospital, Beijing, China, 2Department of Ophthalmology, Peking Union Medical College Hospital, Beijing, China, 3Department of Rheumatology, Peking Union Medical College Hospital, Beijing, China, 4Rheumatology, Peking Union Medical College and Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, Beijing, China

    Background/Purpose: Uveitis is one of the leading causes of morbidity in Behcet’s patients which may result in irreversible vision loss. Evidence is accumulating that interferon…
  • Abstract Number: 1791 • 2018 ACR/ARHP Annual Meeting

    Efficacy of Apremilast for Oral Ulcers Associated with Active Behçet’s Syndrome in a Phase III Study: A Prespecified Analysis By Baseline Patient Demographics and Disease Characteristics

    Gulen Hatemi1, Alfred Mahr2, Mitsuhiro Takeno3, Do-Young Kim4, Melike Melikoglu1, Sue Cheng5, Shannon McCue5, Maria Paris5, Mindy Chen5 and Yusuf Yazici6, 1Istanbul University Cerrahpasa Medical School, Istanbul, Turkey, 2Hospital Saint-Louis, University Paris Diderot, Paris, France, 3Nippon Medical School Graduate School of Medicine, Tokyo, Japan, 4Yonsei University College of Medicine and Severance Hospital, Seoul, Korea, Republic of (South), 5Celgene Corporation, Summit, NJ, 6New York University School of Medicine, New York, NY

    Background/Purpose: Behçet’s syndrome is a chronic, multi-system inflammatory disorder characterized by recurrent oral ulcers (OU) that can be disabling and negatively affect quality of life.…
  • Abstract Number: 1812 • 2018 ACR/ARHP Annual Meeting

    Characterization and Prevalence of Morbus Behçet in Switzerland

    Sabine Adler1, Rahel Villiger2, Lukas Buetikofer3 and Peter M. Villiger4, 1Department of Rheumatology, Immunology and Allergology, Inselspital, University Hospital of Bern, Bern, Switzerland, 2Rheumatology, Immunology and Allergology, University Hospital Bern, Switzerland, Bern, Switzerland, 3Clinical Trials Unit, University of Bern, Bern, Switzerland, 4Rheumatology and Clin Immunol, Bern, Switzerland

    Background/Purpose: To evaluate the clinical presentation of patients with Morbus Behçet (MB) in a cohort from Switzerland and to calculate the prevalence of MB in…
  • Abstract Number: 1794 • 2018 ACR/ARHP Annual Meeting

    Venous Vessel Wall Thickness in Lower Extremity Is Increased in Male Behcet’s Disease Patients

    Fatma Alibaz-Oner1, Rabia Ergelen2, Aydan Mutiş3, Zeynep Erturk1, Ruslan Asadov4, Tulin Ergun5 and Haner Direskeneli6, 1Rheumatology, Marmara University School of Medicine, Istanbul, Turkey, 2Marmara University School of Medicine, Radiology, ISTANBUL, Turkey, 3Marmara University, School of Medicine, Rheumatology, ISTANBUL, Turkey, 4Marmara University School of Medicine, Radiology, Istanbul, Turkey, 5Marmara University, School of Medicine, Dermatology, Istanbul, Turkey, 6Rheumatology, Marmara University, School of Medicine, Istanbul, Turkey

    Background/Purpose: Vascular involvement is seen in up to 40% of the patients with Behcet's Disease (BD), especially in young males and is one of the…
  • Abstract Number: 1813 • 2018 ACR/ARHP Annual Meeting

    Non-Aphthous Beginning As an Independent Risk Factor for the Course of Behçet’s Disease

    Muhammed Aydin1, Bahar Artim-Esen1, Murat Inanc2, Lale Ocal1 and Ahmet Gül1, 1Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey, 2Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul Faculty of Medicine, İstanbul, Turkey

    Background/Purpose: Behçet disease (BD) is a multisystem inflammatory disorder characterized by recurrent manifestations in mucocutaneous tissues, eyes, joints, blood vessels, intestines and brain. Since there…
  • Abstract Number: 2728 • 2017 ACR/ARHP Annual Meeting

    Serum Levels of Interleukin-36 Receptor Antagonist in Behçet’s Patients

    Pelin Ünsal1, Pamir Cerci2, Şükrü Alper Açıkgöz2, Göksal Keskin2 and Ümit Ölmez2, 1Ankara University School of Medicine, Ankara, Turkey, 2Immunology and Allergy, Ankara University School of Medicine, Ankara, Turkey

    Background/Purpose: Behcet's disease (BD) is a systemic vasculitis disorder of unknown etiology with recurrent exacerbations and remissions. The etiopathogenesis of the disease is still unclear.…
  • Abstract Number: 2729 • 2017 ACR/ARHP Annual Meeting

    Surgical Therapies in the Treatment of Pulmonary Artery Involvement in Behcet’s Syndrome

    Hasan Tuzun1, Gul Guzelant2, Ozkan Demirhan3, Buge Oz4, Izzet Fresko2, Vedat Hamuryudan2, Hasan Yazici2 and Emire Seyahi2, 1Istanbul University, Cerrahpasa Medical Faculty, Department of Cardiovascular Surgery, Istanbul, Turkey, 2Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Rheumatology, Istanbul, Turkey, 3Istanbul Bilim University, Medical Faculty, Department of Thoracic Surgery, Istanbul, Turkey, 4Istanbul University, Cerrahpasa Medical Faculty, Department of Pathology, Istanbul, Turkey

    Background/Purpose: The mainstay treatment of pulmonary artery involvement (PAI) in Behcet’s syndrome (BS) is immunosuppresion and corticosteroids (1). The role of surgical intervention in the…
  • Abstract Number: 2732 • 2017 ACR/ARHP Annual Meeting

    Recommendations for the Management of Neuro-Behcet’s Disease By the Japanese National Research Committee for Behcet’s Disease

    Hirotoshi Kikuchi1, Tetsuji Sawada2, Masato Okada3, Mitsuhiro Takeno4, Masataka Kuwana4, Yoshiaki Ishigatsubo5, Izumi Kawachi6, Hideki Mochizuki7, Susumu Kusunoki8 and Shunsei Hirohata9, 1Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan, 2Rheumatology, Tokyo Medical University, Shinjuku Tokyo, Japan, 3Immuno-Rheumatology Center, St. Luke’s International Hospital, Tokyo, Japan, 4Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, 5Department of Internal Medicine and Clinical Immunology, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 6Department of Neurology, Niigata University Medical and Dental Hospital, Niigata, Japan, 7Department of Neurology, Osaka University Graduate School of Medicine, Osaka, Japan, 8Department of Neurology, Kinki University School of Medicine, Osaka, Japan, 9Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Kanagawa, Japan

    Background/Purpose: Central nervous system involvement is one of the most serious complications in Behçet’s disease (BD). This condition is referred to as neuro-Behçet’s disease (NB)…
  • Abstract Number: 2744 • 2017 ACR/ARHP Annual Meeting

    Long-Term Remission in Severe Behcet’s Disease Following Withdrawal of Successful Anti-TNF Treatment

    Petros P Sfikakis1, Aikaterini Arida1, Stylianos Panopoulos2, Kalliopi Fragkiadaki2, George Pentazos3, Katerina Laskari3, Maria Tektonidou1 and Nikos Markomichelakis2, 1First Department of Propaedeutic and Internal Medicine and Joint Rheumatology Program, National and Kapodistrian University of Athens Medical School, athens, Greece, 2First Department of Propaedeutic and Internal Medicine and Joint Rheumatology Program, National and Kapodistrian University of Athens Medical School, Athens, Greece, 3Rheumatology Unit, 1st Dept. of Propaedeutic Internal Medicine, Joined Academic Rheumatology Program, Athens University Medical School, Athens, Greece

    Background/Purpose: Anti-TNF treatment has been shown to be effective in inducing complete remission in many Behcet’s disease (BD) patients with eye, large vessel, intestine and…
  • Abstract Number: 2747 • 2017 ACR/ARHP Annual Meeting

    Long Term Follow-up of Behcet’s Syndrome Patients Treated with Cyclophosphamide

    Mert Gurcan1, Sinem Nihal Esatoglu1, Vedat Hamuryudan1, Caner Saygin2, Didem Saygin3, Serdal Ugurlu4, Emire Seyahi1, Melike Melikoglu1, Izzet Fresko1, Sebahattin Yurdakul1, Hasan Yazici1 and Gulen Hatemi1, 1Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Rheumatology, Istanbul, Turkey, 2Department of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Cleveland, OH, 3Internal Medicine, Department of Internal Medicine, Cleveland Clinic, Cleveland, Cleveland, OH, 4Rheumatology, Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Rheumatology, Istanbul, Turkey

     Background/Purpose: Cyclophosphamide (CYC) remains an important treatment option for Behçet’s syndrome (BS) pts with life threatening conditions such as arterial aneurysms. However, several adverse events…
  • Abstract Number: 2748 • 2017 ACR/ARHP Annual Meeting

    Immunogenicity of Infliximab Among Patients with Behcet’s Syndrome: A Controlled Study

    Sinem Nihal Esatoglu1, Fatma Nihan Akkoc1, Yesim Ozguler1, Fatma Ozbakir2, Okan Kadir Nohut2, Dilsen Cevirgen3, Vedat Hamuryudan1, Ibrahim Hatemi4, Aykut Ferhat Celik5, Hasan Yazici1 and Gulen Hatemi1, 1Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Rheumatology, Istanbul, Turkey, 2Istanbul University, Cerrahpasa Medical Faculty, Central Research Laboratory, Istanbul, Turkey, 3Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of and Rheumatology, Istanbul, Turkey, 4Istanbul University, Cerrahpasa Medical School, Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Gastroenterology, Istanbul, Turkey, 5Istanbul University, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Gastroenterology, Istanbul, Turkey

    Background/Purpose: Immunogenicity of anti-TNFs has been recognized as an important problem that may cause loss of response and adverse events such as infusion reactions. We…
  • Abstract Number: 77 • 2017 ACR/ARHP Annual Meeting

    Platelets Induce IL-1b Production in Human Monocytes through NLRP3 Inflammasome Activation

    Shota Nakano1, Hiroki Mitoma1, Shotaro Kawano1, Shoichiro Inokuchi2, Masahiro Ayano1, Yasutaka Kimoto3, Mitsuteru Akahoshi1, Yojiro Arinobu1, Koichi Akashi1, Takahiko Horiuchi4 and Hiroaki Niro5, 1Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan, 2Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan, 3Department of Internal Medicine, Kyushu University Beppu Hospital, Oita, Japan, 4Department of Internal Medicine, Kyushu University Beppu Hospital, Beppu, Japan, 5Department of Medical Education, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

    Background/Purpose: Recent studies have revealed that platelets play pivotal roles in inflammation in addition to hemostasis. The thrombus induces subsequent local inflammation and reversely the…
  • Abstract Number: 2775 • 2017 ACR/ARHP Annual Meeting

    Critical Role of Neutrophil Extracellular Traps (NETs) in Patients with Behcet’s Disease

    Alexandre LE JONCOUR1,2, Stephane Loyau3, Nicolas Lelay4, Marie-Christine Bouton5, Antoine Dossier6, Anne-Claire Desbois7, Fanny Domont8, Thomas Papo9, Martine Jandrot-Perrus5, Patrice Cacoub10, Nadine Ajzenberg5, David saadoun7 and Yacine Boulaftali2, 1Département Hospitalo-Universitaire Inflammation-Immunopathologie-Biotherapie (DHU i2B), F-75005, Paris, France., National center for Autoimmune and Systemic rare diseases and for Autoinflammatory diseases, Paris, France, 2INSERM 1148, CHU Xavier Bichat, paris, France, 3Unité INSERM 1148, CHU Xavier Bichat, Faris, France, 42. Unité INSERM 1148, CHU Xavier Bichat, paris, France, 5Unité INSERM 1148, CHU Xavier Bichat, paris, France, 63. Service de Médecine Interne, CHU Xavier Bichat, paris, France, 7Département Hospitalo-Universitaire Inflammation-Immunopathologie-Biotherapie, National center for Autoimmune and Systemic rare diseases and for Autoinflammatory diseases, Paris, France, 8Département Hospitalo-Universitaire Inflammation-Immunopathologie-Biotherapie, National center for Autoimmune and Systemic rare diseases and for Autoinflammatory diseases, paris, France, 9Service de Médecine Interne, CHU Xavier Bichat, Paris, France, 10Département de Médecine Interne et Immunologie Clinique, National center for Autoimmune and Systemic rare diseases and for Autoinflammatory diseases, Paris, France

    Background/Purpose: Behçet's disease (BD) is a chronic systemic vasculitis characterised by muco-cutaneous, ocular, gastrointestinal, cerebral recurrent lesions. Venous thrombosis, is a frequent and life-threatening complication.…
  • Abstract Number: 1075 • 2017 ACR/ARHP Annual Meeting

    Higher Frequencies of Lymphocytes Expressing the Natural Killer Group 2D Receptor and Cytotoxic Potential of NK Cells in Patients with Behcet Disease

    Martina Bonacini1, Stefania Croci1, Alessandra Soriano2,3, Eleonora Calò1, Alessandro Zerbini1, Luca Cimino4, Francesco Muratore2,5, Luigi Fontana6, Maria Parmeggiani1 and Carlo Salvarani2,5, 1Unit of Clinical Immunology, Allergy and Advanced Biotechnologies, Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia, Italy, Reggio Emilia, Italy, 2Unit of Rheumatology, Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia, Italy, Reggio Emilia, Italy, 3Campus Bio-Medico, University of Rome, Italy, Roma, Italy, 4Unit of Ocular Immunology, Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia, Italy, Reggio Emilia, Italy, 5University of Modena and Reggio Emilia, Italy, Modena, Italy, 6Unit of Ophthalmology, Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia, Italy, Reggio Emilia, Italy

    Background/Purpose: Behçhet disease (BD) is a rare, systemic, inflammatory disorder with multiorgan damage and various clinical manifestations such as oral ulcers, genital ulcers and uveitis.…
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