Results 11 to 20 of about 118,654 (333)

Mechanisms, biomarkers and targets for adult-onset Still’s disease

Nature Reviews Rheumatology, 2018
Adult-onset Still’s disease (AoSD) is a rare but clinically well-known, polygenic, systemic autoinflammatory disease. Owing to its sporadic appearance in all adult age groups with potentially severe inflammatory onset accompanied by a broad spectrum of ...
E. Feist, S. Mitrovic, B. Fautrel
semanticscholar   +3 more sources

Difficulties in diagnosis and treatment of adult-onset Still's disease concurrent with pericardial effusion as a leading clinical manifestation [PDF]

Современная ревматология, 2016
The paper considers a case of adult-onset Still's disease that occurred as acute pericarditis, two-spike hectic fever, and neutrophilic leukocytosis in a young man.
V. Yu. Myachikova, A. L. Maslyansky, I. Z. Gaydukova, A. N. Novikova, D. V. Karpova, E. V. Shlyakhto   +5 more
doaj   +3 more sources

Coincidence or association: Adult‐onset Still's disease following HPV vaccine [PDF]

Clinical Case Reports
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 the well ...
Muhammad Ahmed, Kaab Husain, Arqam Husain, Sameer Syed, Mahfujul Z. Haque, Alireza Meysami   +5 more
doaj   +2 more sources

Macrophage activation syndrome complicating early course of adult-onset Still’s disease [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2021
Introduction. Adult-onset Still’s disease is a rare inflammatory disorder of unknown etiology. It can be complicated by macrophage activation syndrome, a potentially life-threatening condition. While macrophage activation syndrome and adult-onset Still’s
Božić Ksenija, Elez Marija, Glišić Branislava   +2 more
doaj   +1 more source

Still’s disease continuum from childhood to elderly: data from the international AIDA Network Still’s disease registry

RMD Open, 2023
Objective Still’s disease is more frequently observed in the paediatric context, but a delayed onset is not exceptional both in the adulthood and in the elderly.
Micol Frassi, Marcello Govoni, Annamaria Iagnocco, Florenzo Iannone, Paola Triggianese, Corrado Campochiaro, Sara Monti, Maria G Tektonidou, Eduardo Martin-Nares, Piero Ruscitti, Roberto Giacomelli, Luca Cantarini, Giuseppe Lopalco, Lorenzo Dagna, Francesco Carubbi, Alma Nunzia Olivieri, Antonio Vitale, Ombretta Viapiana, Fatma Alibaz-Öner, Haner Direskeneli, Petros P Sfikakis, Giacomo Emmi, Claudia Fabiani, Gabriele Simonini, Francesco Ciccia, Elena Bartoloni, Alessandro Tomelleri, Daniela Iacono, Riza Can Kardas, Bruno Frediani, Benson Ogunjimi, Amato de Paulis, Onorina Berardicurti, Alessandro Conforti, Ilenia Di Cola, Anastasios Karamanakos, Katerina Laskari, Abdurrahman Tufan, Stefania Costi, José Hernández-Rodríguez, Lampros Fotis, Jurgen Sota, Antonio Gidaro, Ewa Wiesik-Szewczyk, Gian Domenico Sebastiani, Jiram Torres-Ruiz, Paolo Sfriso, Giovanni Conti, Luca Navarini, Francesco La Torre, Samar Tharwat, Andrea Hinojosa-Azaola, Alberto Lo Gullo, Valeria Caggiano, Ibrahim A Almaghlouth, Kazi Asfina, Gafaar Ragab, Maria Cristina Maggio, Joanna Makowska, Emanuela Del Giudice, Armin Maier, Sukran Erten, Henrique A Mayrink Giardini, Maria Morrone, Isabele Parente de Brito Antonelli, Marilia Ambiel Dagostin, Martina Patrone, Fehaid Alanazi, Carla Gaggiano, Hamit Kucuk, Ayman Abdel-Monem Ahmed Mahmoud, Katerina Kourtesi, Maria Tarsia, Verónica Gómez-Caverzaschi, Angela Mauro, Alberto Balistreri   +75 more
doaj   +1 more source

Adult-onset Still's disease in focus: Clinical manifestations, diagnosis, treatment, and unmet needs in the era of targeted therapies.

Seminars in Arthritis & Rheumatism, 2021
BACKGROUND Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology, characterized by a clinical triad of high spiking fever, arthralgia (± arthritis), and evanescent skin rash.
P. Efthimiou, A. Kontzias, Peter Hur, K. Rodha, G. Ramakrishna, P. Nakasato   +5 more
semanticscholar   +1 more source

Adult Onset Still’s Disease [PDF]

Journal of Evolution of Medical and Dental Sciences, 2019
Adult-onset Still’s disease (AoSD) is a rare but clinically well-known, polygenic, systemic autoinflammatory disease. It is typically characterized by four main (cardinal) symptoms: spiking fever ≥39 °C, arthralgia or arthritis, skin rash, and hyperleukocytosis (≥10,000 cells/mm(3)). However, many other clinical features are possible, and it can appear
Bimal K. Agrawal, Gaurav Aggarwal, Deepanshu Khanna   +2 more
  +5 more sources

Adult Still’s disease – a multidisciplinary disease [PDF]

Archives of the Balkan Medical Union, 2021
Introduction. Adult-onset Still’s disease is a rare systemic autoinflammatory disorder of unknown etiology, characterized by persistent fever, maculopapular skin rash, and arthritis or arthralgia.
Leonid I. DVORETSKY, Daria V. NOVIKOVA, Anna V. TORGASHNA, Alla M. KOVRIGINA, Tatiana N. MOISEEVA, Roza M. VAKOLYUK, Maria A. KARNAUSHKINA   +6 more
doaj   +1 more source

Oral mucosa lesions as atypical manifestation of adult-onset Still´s disease [PDF]

Anais Brasileiros de Dermatologia, 2018
: Adult-onset Still's disease is a systemic inflammatory disorder of unknown etiology, characterized by skin rash, spiking fever, arthralgias or arthritis, and leukocytosis. The typical skin rash is evanescent, salmon-pink, nonpruritic and maculopapular,
María Lorena Brance, Eldo Luis Neffen
doaj   +1 more source

Adult-onset Still’s Disease: A Case Report

Journal of Nepal Medical Association, 2023
Pyrexia of unknown origin refers to a fever of over 38.3°C on multiple occasions for at least three weeks without a known aetiology, even after a week of hospitalization.
Bikash Karki, Niranjan K C, Arun Kumar Mahato, Saksham Kandel, Prakash Acharya   +4 more
doaj   +1 more source