Results 11 to 20 of about 2,098 (173)

Paraneoplastic Adult-Onset Still's Disease Caused by Mediastinal Lymph Node Carcinoma of Unknown Primary Site, Most Likely Lung Adenocarcinoma. [PDF]

Int J Rheum Dis
International Journal of Rheumatic Diseases, Volume 29, Issue 8, August 2026.
Taniguchi Y, Okada D.
europepmc   +2 more sources

Refractory Relapsing-Remitting Adult-Onset Still's Disease in an Adolescent Female: A Rare Case Report. [PDF]

Clin Case Rep
ABSTRACT Adult‐onset Still's disease (AOSD) is a rare systemic autoinflammatory condition that presents with symptoms such as episodic fevers, a transient rash, inflammatory arthritis, and significant systemic inflammation. Diseases that have a relapsing–remitting clinical course can be challenging to diagnose and treat. We present a case of an 18 year
Nafian T, Bhuiyan MMA, Aftab KA, Murshed KM, Azad MAK.   +4 more
europepmc   +2 more sources

Large-Scale Autoantibody Reactome Analysis Reveals Shared and Specific Signatures Across Different Immune-Mediated Inflammatory Diseases. [PDF]

ACR Open Rheumatol
Objective The shared and disease‐specific mechanisms across the immune‐mediated inflammatory diseases (IMIDs) spectrum remains incompletely characterized, despite the recognized role of autoantibodies as important indicators of immune tolerance breakdown and immune dysregulation. Methods Autoantibody reactome profiling of IgG and IgA autoantibodies was
Bai Z, Yu B, Wei Z, Xiao P, Zhan M, Li M, Wang F, Cheng Y, Zhao M, Zhang C, Zhang X, Yu X, Liu Y.   +12 more
europepmc   +2 more sources

Towards a standard design language for AOSD [PDF]

Proceedings of the 1st international conference on Aspect-oriented software development - AOSD '02, 2002
For aspect-oriented software development (AOSD) to live up to being a software engineering method, there must be support for the separation of crosscutting concerns across the development lifecycle. Part of this support is traceability from one lifecycle phase to another.This paper investigates the traceability between one particular AOSD design-level ...
Siobhán Clarke, Robert J. Walker
openaire   +2 more sources

Atypical Persistent Pruritic Hyperpigmented Plaques in Adult-Onset Still's Disease: A Case Report From Uganda. [PDF]

Clin Case Rep
Atypical Persistent hyperpigmented cutaneous lesions associated with adult‐onset Still's disease. ABSTRACT We report a case of adult‐onset Still's disease (AOSD) in a 30‐year‐old Ugandan man presenting with migratory polyarthralgia, intermittent fever, lymphadenopathy, and atypical persistent pruritic hyperpigmented plaques.
Sandeyl AA, Mirembe SK, Byaruhanga K, Abdi FD, Hersi AG, Kamyuka LK, Mswelo VE, Hassan RY.   +7 more
europepmc   +2 more sources

Neutrophil extracellular trap-induced intermediate monocytes trigger macrophage activation syndrome in adult-onset Still’s disease

BMC Medicine, 2023
Background Adult-onset Still’s disease (AOSD) is a systemic autoinflammatory disease characterized by innate immune system activation, with a high risk for macrophage activation syndrome (MAS).
Jinchao Jia, Mengyan Wang, Yuning Ma, Jianfen Meng, Dehao Zhu, Xia Chen, Hui Shi, Yue Sun, Honglei Liu, Xiaobing Cheng, Yutong Su, Junna Ye, Huihui Chi, Tingting Liu, Zhuochao Zhou, Fan Wang, Longfang Chen, Da Yi, Yu Xiao, Chengde Yang, Jialin Teng, Qiongyi Hu   +21 more
doaj   +1 more source

Clinical characteristics and outcome of elderly onset adult-onset Still's disease: A 10-year retrospective study

Journal of Translational Autoimmunity, 2023
Objective: Our objective was to retrospectively analyze the clinical characteristics and outcome of adult-onset Still's disease (AOSD) patients with elderly onset.
Sheng Li, Shuni Ying, Juan Bai, Yuqian Wang, Changyi Yang, Qingmiao Sun, Hong Fang, Jianjun Qiao   +7 more
doaj   +1 more source

Adult-Onset Still Disease (AOSD) [PDF]

The Journal of the American Board of Family Medicine, 2010
Adult-onset Still disease (AOSD) is an uncommon clinical entity that predominantly affects young adults. One of the most common presentations of the disease is fever of unknown origin. Early diagnosis can be difficult because fever of unknown origin is more commonly seen with other conditions such as malignancy or infection.
Egambaram, Senthilvel, Aphrodite, Papadakis, Michael, McNamara, Iyabode, Adebambo   +3 more
openaire   +2 more sources

Adjunctive Therapeutic Plasma Exchange in Refractory Adult-Onset Still's Disease Complicated by Secondary Macrophage Activation Syndrome: A Single-Center Experience. [PDF]

Ther Apher Dial
ABSTRACT Introduction Adult‐onset Still's disease (AOSD) complicated by macrophage activation syndrome (MAS) carries substantial mortality. The role of therapeutic plasma exchange (TPE) remains uncertain. Methods We retrospectively analyzed patients with AOSD‐MAS treated with TPE at a single‐center.
Ueda M, Saito T, Mizobuchi M, Shimomura T, Kawamori S, Kawanishi M, Hattori N, Sugiyama J, Tsubata S, Horiguchi H, Abe K, Iida N, Kajio Y, Oguro N, Yanai R, Honda H.   +15 more
europepmc   +2 more sources

B cell subsets in adult-onset Still’s disease: potential candidates for disease pathogenesis and immunophenotyping

Arthritis Research & Therapy, 2023
Background Adult-onset Still’s disease (AOSD) is a systemic autoinflammatory disorder of unknown etiology. B cells are critical participants in different rheumatic diseases, and their roles in AOSD are rarely investigated.
Xiangyu Fang, Hua Ye, Yang Xie, Chaonan Wei, Shuyan Liu, Haihong Yao, Zhanguo Li, Yuan Jia, Fanlei Hu   +8 more
doaj   +1 more source