Results 81 to 90 of about 8,508 (236)

Circulating Fetuin‐A concentrations in rheumatic diseases: a systematic review and meta‐analysis

European Journal of Clinical Investigation, Volume 55, Issue 5, May 2025.
In this systematic review with meta‐analysis, we identified 19 eligible studies to determine whether there is any change in Fetuin‐A (FtA) concentrations in patients with rheumatic diseases. We observed a significant decrease in FtA concentrations in RD patients (standardized mean difference, SMD = −.91; 95% CI −1.43 to −.39, p = .001).
Biagio Di Lorenzo, Stefano Zoroddu, Arduino A. Mangoni, Panagiotis Paliogiannis, Gian Luca Erre, Ciriaco Carru, Angelo Zinellu   +6 more
wiley   +1 more source

Failure of tocilizumab in treating two patients with refractory SAPHO syndrome: a case report

Journal of International Medical Research, 2018
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare autoinflammatory disease with no standard treatment. Interleukin (IL)-6 inhibitors represent a novel therapeutic option for rheumatoid arthritis and some autoinflammatory ...
Xiao-Chuan Sun, Shuang Liu, Chen Li, Shuo Zhang, Mu Wang, Xiao-Hua Shi, Wei-Xin Hao, Wen Zhang   +7 more
doaj   +1 more source

Longinus, Sappho’s Ode, and the Question of Sublimity [PDF]

, 2005
De prime abord, cet article peut sembler porter sur les attitudes à l’endroit de l’autorité des anciens, mais il porte en fait sur l’ironie du ton et sur la difficulté qu’on peut avoir à la déceler, même quand le locuteur ou
Cochran, Peter
core   +1 more source

Successful Treatment of Refractory Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO) Syndrome with Baricitinib, a Janus Kinase Inhibitor

Clinical, Cosmetic and Investigational Dermatology
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome, a rare immune-mediated inflammatory disease, poses diagnostic and therapeutic challenges owing to its multi-system involvement, high heterogeneity, and lack of specific laboratory ...
Jianqiu Yang, Chunyu Yuan, Shengru Zhou, Zhicheng Teng, Min Li   +4 more
semanticscholar   +1 more source

Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT This case highlights the possibility that Immunoglobulin G4‐related disease (IgG4‐RD) lesions can also occur in the sternoclavicular joint. If a neoplastic lesion is found in the sternoclavicular joint, a biopsy should be attempted to diagnose IgG4‐RD as a differential.
Remi Mizuta, Shinnosuke Takemoto, Mutsumi Ozasa, Sawana Ono, Takahito Fukuda, Ryuta Tagawa, Fumiko Hayashi, Kazumasa Akagi, Hiromi Tomono, Hirokazu Taniguchi, Midori Matsuo, Hiroshi Gyotoku, Takahiro Takazono, Hiroshi Ishimoto, Noriho Sakamoto, Keitaro Matsumoto, Yasushi Obase, Tomoya Nishino, Hiroshi Mukae   +18 more
wiley   +1 more source

SAPHO syndrome

Rheumatology, 2021
Peng Xu, Gaofeng Yi, Jun Li
openaire   +3 more sources

Sapho syndrome. Tune-up on a clinical case in the CHPR.

Revista de la Asociación Argentina de Ortopedia y Traumatología, 2018
Sapho syndrome involves synovitis, acne, pustulosis, hiperostosis and osteitis. It is recognized since 1987 as a sero negative spondiloartrhopaty.
Juan Miguel Del Castillo Bellón, Nicolás Casales, Claudio Silveri   +2 more
doaj   +1 more source

Considerations for defining and diagnosing generalized pustular psoriasis

Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 3, Page 487-497, March 2025.
Generalized pustular psoriasis (GPP) is a rare chronic skin disease with inconsistent definitions and diagnostic criteria. It is characterized by widespread pustules and erythema, which are often accompanied by other signs and symptoms. Cases of suspected GPP may benefit from laboratory testing to assess organ function as well as genetic and ...
Vimal H. Prajapati, Charles W. Lynde, Melinda J. Gooderham, H. Chih‐ho Hong, Mark G. Kirchhof, Perla Lansang, Julien Ringuet, Irina Turchin, Ron Vender, Jensen Yeung, Kim A. Papp   +10 more
wiley   +1 more source

Successful Treatment of Refractory Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO) Syndrome With Tofacitinib: A Case Report

Cureus
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is primarily manifested by persistent inflammation affecting the musculoskeletal system and the skin. The treatment of SAPHO syndrome remains a challenge.
Mustafa Alhayali
semanticscholar   +1 more source

SÍNDROME SAPHO: A PROPÓSITO DE UN CASO

Revistas Argentina de Medicina, 2019
El síndrome SAPHO es un cuadro clínico caracterizado por sinovitis, acné, pustulosis, hiperostosis y osteítis. Generalmente es un síndrome benigno, autolimitado y crónico, con períodos de exacerbaciones y remisiones.
María F. Sola, José Gamarra, Marcelo J. Caldas, Agustina Busso Vanrell, Marina Martínez, Constanza Giardullo, Rodrigo García, Marcelo Villaverde   +7 more
doaj   +2 more sources