Results 41 to 50 of about 118,654 (333)

Adult-onset Still’s disease: A disease at the crossroad of innate immunity and autoimmunity

Frontiers in Medicine, 2022
Adult-onset Still’s disease (AOSD) is a rare disease affecting multiple systems and organs with unknown etiology, and the clinical symptoms are usually described as spiking fever, arthritis, evanescent salmon-pink eruptions, lymphadenopathy, splenomegaly,
Shijia Rao, L. Tsang, Ming Zhao, W. Shi, Q. Lu   +4 more
semanticscholar   +1 more source

Adult-Onset Still’s Disease Presenting as Macrophage-Activation Syndrome With Critical Illness in the Third Trimester of Pregnancy: A Case Report

Critical Care Explorations, 2021
BACKGROUND:. We report a case of a young woman with adult-onset Still’s disease presenting as macrophage-activation syndrome complicated by shock and respiratory failure during the third trimester of pregnancy. CASE SUMMARY:. A previously healthy 26-year-
Andrew T. Peters, MD, Michelle H. Prickett, MD   +1 more
doaj   +1 more source

Pregnancy-Associated Onset of Adult-Onset Still's Disease [PDF]

American Journal of Perinatology Reports
Nawras Zayat, Avish Arora, Joselle O'Brien, Japjot Bal, Rebekah Sugarman, Leeshun Rivera, Amir Shamshirsaz, Kavita Vani, Dimitrios S. Mastrogiannis   +8 more
doaj   +2 more sources

Macrophage Activation Syndrome [PDF]

, 2015
Macrophage activation syndrome (MAS) is a potentially life-threatening complication of rheumatic diseases such as systemic juvenile idiopathic arthritis (sJIA) and systemic lupus erythematosus.
Clarke, Sarah L N, Ramanan, Athimalaipet V, Sen, Ethan S   +2 more
core   +2 more sources

A case of adult‐onset Still's disease in a patient after a car accident

Clinical Case Reports, 2023
Key Clinical Message Adult‐onset Still's disease is a rare inflammatory condition with diverse clinical features. Yamaguchi criteria aid diagnosis, and pleural effusion and elevated ferritin levels are important markers.
Feride Yaman, Ali Kimiaei
doaj   +1 more source

Biomarkers for adult-onset Still’s disease

Научно-практическая ревматология, 2022
Adult-onset Still’s disease (AOSD) is a rare complex autoinflammatory disease of unknown etiology. The main problem, practitioners have been facing with when researching AOSD, is the lack of developed approaches to assessing the activity of the disease ...
V. Yu. Myachikova, O. Yu. Tkachenko, S. V. Lapin, E. S. Kuvardin, A. L. Maslyanskiy   +4 more
doaj   +1 more source

Increased neutrophil extracellular traps activate NLRP3 and inflammatory macrophages in adult-onset Still’s disease

Arthritis Research & Therapy, 2019
BackgroundAdult-onset Still’s disease (AOSD) is a systemic inflammatory disease characterized by neutrophilia and NLRP3 inflammasome and macrophage activation. We investigated the role of neutrophil extracellular traps (NETs) in the pathogenesis of AOSD,
Qiong-yi Hu, Hui Shi, Ting Zeng, Honglei Liu, Yutong Su, Xiaobing Cheng, Junna Ye, Yufeng Yin, Meng-ru Liu, Hui Zheng, Xinyao Wu, Huihui Chi, Zhuochao Zhou, Jinchao Jia, Yue Sun, Jialin Teng, Chengde Yang   +16 more
semanticscholar   +1 more source

Adult-onset Still’s disease

Journal of Medical and Scientific Research, 2015
A 24-year-old male presented with fever, sore throat, and arthralgias for duration of 4 weeks. Fever was high grade, intermittent, associated with maculopapular rash. He was admitted in outside hospital and was started on antibiotics, antituberculosis treatment (ATT), and anti-malarials. The patient was discharged without any improvement.
Srinivas, Sarath Chandra Mouli, Sravan Kumar   +2 more
openaire   +4 more sources

Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report

Journal of Medical Case Reports, 2012
Introduction Lymphadenopathy is found in about 65% of patients with adult-onset Still’s disease and is histologically characterized by an intense, paracortical immunoblastic hyperplasia. Adult-onset Still’s disease has not been previously described as an
Assimakopoulos Stelios F, Karamouzos Vassilios, Papakonstantinou Christos, Zolota Vassiliki, Labropoulou-Karatza Chryssoula, Gogos Charalambos   +5 more
doaj   +1 more source

Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome [PDF]

, 1994
Contains fulltext : 4767.pdf (publisher's version ) (Open ...
Boom, B.W., Drenth, J.P.H., Meer, J.W.M. van der, Toonstra, J.   +3 more
core   +2 more sources