Results 31 to 40 of about 4,960 (303)

Association Between Peripheral Eosinophilia and Clinical Characteristics of Adult-onset Still’s Disease with Persistent Eruption: A Retrospective Study

Acta Dermato-Venereologica, 2021
Persistent eruption occurs in a subset of patients with adult-onset Still’s disease. In our experience, a considerable proportion of these patients present with peripheral eosinophilia.
Jia-Wei Liu, Tian Chen, Wei Liu, Ru-Xuan Chen, Yue-Tong Qian, Yan Tan, Dong-Lai Ma   +6 more
doaj   +1 more source

An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis [PDF]

, 2010
Tuberculosis (TB), caused by infection with Mycobacterium tuberculosis (M. tuberculosis), is a major cause of morbidity and mortality worldwide and efforts to control TB are hampered by difficulties with diagnosis, prevention and treatment 1,2.
A Falk, AM Cooper, AM Cooper, Anne O’Garra, Asuncion Mejias, C Auffray, C Dye, C Manca, C Manca, C Telesca, CE Barry III, Charles Quinn, Christine M. Graham, D Chaussabel, D Ordway, D Salisbury, Damien Chaussabel, DB Young, Derek Blankenship, EB Eruslanov, EC Baechler, F Allantaz, Finlay W. McNab, Jacques Banchereau, Jason Skinner, JL Casanova, JL Flynn, John J. Cush, JS Beck, Katalin A. Wilkinson, L Bennett, M Jacobsen, Matthew P. R. Berry, MI Ardura, O Ramilo, Octavio Ramilo, Onn M. Kon, R Mistry, R Pankla, Ranju Dhawan, Robert J. Wilkinson, Romain Banchereau, SH Kaufmann, Susannah A. A. Bloch, SY Eum, T Decker, Tolu Oni, V Pascual, Virginia Pascual, Zhaohui Xu   +49 more
core   +1 more source

Persistent pruritic papules and plaques: a characteristic histopathologic presentation seen in a subset of patients with adult-onset and juvenile Still's disease [PDF]

, 2010
Background: ‘Persistent pruritic papules and plaques' of Still's disease represents a recently described eruption seen in a subset of patients. Most cases reported in the literature to date have been associated with adult-onset Still's disease.
Affleck, Bywaters, Fautrel, Lee, Lűbbe, Mehrpoor, Prendiville, Ravelli, Suzuki, Wolgamot   +9 more
core   +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

Soluble interleukin-18 receptor complex is a novel biomarker in rheumatoid arthritis [PDF]

, 2011
Introduction There has been no report in the literature of a soluble form of interleukin (IL)-18 receptor α (IL-18Rα). In this study, we evaluated the levels and characteristics of soluble IL-18Rα (sIL-18Rα) in the sera of patients with ...
Satoko Takei, Tomoaki Hoshino, Kazuko Matsunaga, Yuki Sakazaki, Masanori Sawada, Hanako Oda, Shin-ichi Takenaka, Haruki Imaoka, Takashi Kinoshita, Seiyo Honda, Hiroaki Ida, Taka-aki Fukuda, Hisamichi Aizawa   +12 more
core   +1 more source

ADULT-ONSET STILL’S DISEASE: ASPECTS OF THE HEMATOLOGY CLINIC

Сибирский научный медицинский журнал, 2019
The analysis of literature data on modern approaches in the diagnosis and treatment of adult-onset Still’s disease has been performed. A clinical case of Still’s disease associated with lymphadenopathy syndrome was demonstrated.
M. M. Agakishiev, I. I. Mulina, A. M. Popova, I. N. Nechunaeva, L. M. Maslova, I. B. Kovynev, T. I. Pospelova   +6 more
doaj   +1 more source

Interleukin-18 [PDF]

, 2003
Interleukin-18 (IL-18), a recently described member of the IL-1 cytokine superfamily, is now recognized as an important regulator of innate and acquired immune responses.
Gracie, J.A., McInnes, I.B., Robertson, S.E.   +2 more
core   +1 more source

Pneumonitis in Adult Onset Still’s Disease: Uncommon or Under Diagnosed?

Acta Médica Portuguesa, 2017
The adult onset Still’s Disease is an uncommon entity characterized by multiple clinical manifestations. Pneumonitis, less often considered, deserves particular emphasis given the need for differential diagnosis and because it can progress to severe ...
Silvia Fernandes, Margarida Almeida, José Alberto Pereira da Silva, José Carlos Romeu   +3 more
doaj   +1 more source

Association between adult-onset still’s disease and COVID-19: A report of two cases and brief review

SAGE Open Medical Case Reports
Adult-onset still’s disease is a rare multisystemic autoinflammatory disorder with an estimated annual incidence of 0.16–0.62 per 100,000 individuals worldwide. It is typically considered a diagnosis of exclusion.
Sarah Fet-He, Gabriel Ibarra Lecompte, Alejandro José Quiroz Alfaro   +2 more
doaj   +1 more source

Unheard and Under‐Supported: Health‐Related Quality of Life in Children, Adolescents, and Young Adults With Sickle Cell Disease

Pediatric Blood &Cancer, EarlyView.
Abstract Background Sickle cell disease (SCD) is an autosomal recessive hemoglobinopathy affecting millions of individuals worldwide. The clinical expression and psychosocial burden of SCD vary widely across geographical, cultural, and healthcare system contexts, underscoring the need for setting‐specific approaches to assessment.
Desiré Fantasia, Giulia Reggiani, Elizabeth J. Maran, Maria Elisa Delle Fave, Ilaria Baido, Anna Chiara Frigo, Maria Paola Boaro, Raffaella Colombatti   +7 more
wiley   +1 more source