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Elderly-onset adult Still's disease. [PDF]

Reumatologia, 2021
Adult-onset Still’s disease is a rare inflammatory disorder usually affecting young adults. Elderly-onset Still’s disease (EOSD) is reported in some cases, commonly in Japan, the USA and Europe.
Mzabi A, Fakhfakh R, Thabet M, Hassine IB, Anoun J, Karmani M, Ben Fredj F, Laouani C.   +7 more
europepmc   +2 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. This triad of symptoms is usually accompanied by lymphadenopathy, hepatosplenomegaly, and various systemic manifestations. In the absence of adequate therapy,
Leonid I. DVORETSKY, Daria V. NOVIKOVA, Anna V. TORGASHNA, Alla M. KOVRIGINA, Tatiana N. MOISEEVA, Roza M. VAKOLYUK, Maria A. KARNAUSHKINA   +6 more
openaire   +3 more sources

Septic arthritis or adult-onset still's disease: analyzing the causes of recurrent fever after arthroscopic combined anterior cruciate ligament and posterior cruciate ligament reconstruction: a case report. [PDF]

BMC Musculoskelet Disord
Background Adult-onset still’s disease and septic arthritis share similar symptoms—fever, joint pain, and limited mobility—making postoperative diagnosis difficult after combined anterior cruciate ligament and posterior cruciate ligament reconstruction ...
Tian Z, Ni J, Wei W, Song Q, Liu S, Wang D, Li R, Wang D, Chen Z, Jia Z, Jiang J, Shi Z.   +11 more
europepmc   +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

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

Adult-onset Still’s disease

Rheumatology International, 2009
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder characterised by high spiking fever, an evanescent salmon pink rash and arthritis, frequently accompanied by sore throat, myalgias, lymphadenopathies, splenomegaly and neutrophilic leukocytosis.
Bagnari V, COLINA, Matteo, CIANCIO, GIovanni, GOVONI, Marcello, TROTTA, Francesco   +4 more
openaire   +4 more sources

The association between adult-onset Still’s disease and collapsing glomerulopathy: a case report

Journal of Medical Case Reports, 2022
Background Collapsing glomerulopathy, characterized by marked hypertrophy and hyperplasia of the podocytes with eventual collapse of the glomerular tuft, is an important cause of end-stage renal disease. Among the many causes of collapsing glomerulopathy,
Matas Orentas, Nilam Patel, Roger Rodby, Sobia Hassan   +3 more
doaj   +1 more source

Therapy with canakinumab for adult-onset still's disease

Научно-практическая ревматология, 2019
Still's disease in children (systemic-onset juvenile idiopathic arthritis, SoJIA) and in adults (adult-onset Still's disease) are considered as non-familial systemic autoinflammatory diseases of unknown etiology driven by similar immunopathogenetic ...
E. L. Nasonov
doaj   +1 more source