Zobrazeno 1 - 10
of 3 092
pro vyhledávání: '"ADULT-ONSET STILL'S DISEASE"'
Autor:
Indigo Milne, Rhea Kanwar, Whitney Martin, Daniel Egert, Allison Leisgang, Shirley A. Albano-Aluquin, Maria P. Henao, Christine Kreider, Paddy Ssentongo
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-7 (2024)
Abstract Introduction Adult-onset Still’s disease is a rare systemic autoinflammatory disease. We present a case of a young man with a constellation of symptoms and myopericarditis as a complication of this disease. Case A 36-year-old Hispanic man
Externí odkaz:
https://doaj.org/article/6688c0eadaf04a3282641712a38287f6
Autor:
Shuhei Yoshida, Yuya Fujita, Tomohiro Koga, Haruki Matsumoto, Yuya Sumichika, Kenji Saito, Shuzo Sato, Tomoyuki Asano, Masao Kobayakawa, Masashi Mizokami, Masaya Sugiyama, Kiyoshi Migita
Publikováno v:
Immunological Medicine, Pp 1-12 (2024)
This study aimed to identify biomarkers to distinguish adult-onset Still’s disease (AOSD) and to predict disease phenotypes. In total, 49 patients diagnosed with AOSD and 200 patients with common diseases (controls) were included in the analysis. T
Externí odkaz:
https://doaj.org/article/0acb55495150446ba992b8fd8d446a46
Publikováno v:
Immunological Medicine, Pp 1-5 (2024)
Elevated liver enzymes are commonly observed among adult-onset Still’s disease (AOSD), but severe acute liver failure is extremely rare. Although severe acute liver failure associated with AOSD poses a life-threatening condition, the appropriate tr
Externí odkaz:
https://doaj.org/article/1e4f7681f0c5433db2b8328296cd726c
Autor:
Yannick Laurent Tchenadoyo Bayala, Issa Ouedraogo, Hervé Eric Mourfou, Bakoubassé Aïssata Son, Wendyam Nadège Yameogo, Ismael Ayouba Tinni, Wendlassida Joëlle Stéphanie Zabsonré Tiendrébéogo, Dieu‐Donné Ouedraogo
Publikováno v:
Clinical Case Reports, Vol 12, Iss 11, Pp n/a-n/a (2024)
Key Clinical Message Differentiating Adult‐Onset Still's Disease (AOSD) from lymphoma is challenging. A 23‐year‐old female presented with polyarthralgia, fever, rash, lymphadenopathy, and abnormal labs. She met AOSD criteria and was diagnosed w
Externí odkaz:
https://doaj.org/article/5794c88c253b4cc08df6ba74e93b49aa
Autor:
Diana Prieto-Peña, Eztizen Labrador-Sánchez, Rafael B. Melero-González, Fred Antón-Pagés, Natalia Palmou-Fontana, Carmen Alvarez-Reguera, Nerea Paz-Gandiaga, Ricardo Blanco
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
ObjectiveNext-generation sequencing (NGS) panels are increasingly used for the diagnosis of monogenic systemic autoinflammatory diseases (SAIDs). However, their role in patients with adult-onset Still’s disease (AOSD) remains unknown. This study ai
Externí odkaz:
https://doaj.org/article/57501b47f5ba4b6894258b6a34a1de10
Autor:
Berivan Bitik, Mustafa Şenturk, Seda Kibaroglu, Tulin Yildirim, Mehmet Engin Tezcan, Pınar Zeyneloglu, Ahmet Eftal Yucel
Publikováno v:
European Journal of Case Reports in Internal Medicine (2024)
Background: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disease characterized by fever, rash, arthritis, and multi-organ involvement. Macrophage activation syndrome (MAS), a serious complication of AOSD, poses significant dia
Externí odkaz:
https://doaj.org/article/5a24b402a142486ea94fd4f8754051bb
Autor:
Patrick Brossard, Christian Laveille
Publikováno v:
Rheumatology and Therapy, Vol 11, Iss 3, Pp 869-880 (2024)
Abstract Introduction Emapalumab is a fully human monoclonal antibody that targets free and receptor-bound interferon-gamma (IFNγ), neutralizing its biological activity. IFNγ levels differ by orders of magnitude between patients with primary hemoph
Externí odkaz:
https://doaj.org/article/3269a63113544c5fb3eb1d9820a75c89
Publikováno v:
Современная ревматология, Vol 18, Iss 1, Pp 47-53 (2024)
Adult-onset Still's disease (AOSD) is a systemic autoinflammatory disease of unknown etiology characterized by clinical manifestations such as fever, non-stable maculopapular rash, arthritis and/or arthralgias and leukocytosis with neutrophilia.Objec
Externí odkaz:
https://doaj.org/article/216df5ece69248c89e5b70dc56ce7c9d
Autor:
Valentina Myachikova, Igor Kudryavtsev, Artem Rubinstein, Arthur Aquino, Dmitry Isakov, Alexey Golovkin, Alexey Maslyanskiy
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 2, Pp 1177-1191 (2024)
Adult-onset Still’s disease (AOSD) is a complex systemic inflammatory disorder, categorized as an ‘IL-1 driven’ inflammasomapathy. Despite this, the interaction between T and B cells remains poorly understood. We conducted a study, enrolling 7
Externí odkaz:
https://doaj.org/article/e83c9a1ddf364f8e9745ee05db004c94
Publikováno v:
Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Key Clinical Message This case details adult‐onset Still's disease (AOSD) onset post‐human papillomavirus (HPV) vaccination and acute gastroenteritis. The timing of HPV vaccine and vaccine‐autoimmune disease literature may potentially confound
Externí odkaz:
https://doaj.org/article/e68080ea6a5a49afa780dc739e28ce50