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Ruxolitinib for Refractory Macrophage Activation Syndrome Complicating Adult-Onset Still's Disease.
Levy, Ofer; Apel, Arie; Alhdor, Hossam; Mizrachi, Avraham; Agmon-Levin, Nancy; Koren-Michowitz, Maya; Amit-Vazina, Mirit.
Afiliação
  • Levy O; Shamir Medical Center, Internal Medicine B, Rheumatology Unit, Zerifin, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Apel A; Shamir Medical Center, Department of Hematology, Zerifin, Israel.
  • Alhdor H; Shamir Medical Center, Internal Medicine B, Zerifin, Israel.
  • Mizrachi A; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Shamir Medical Center, Internal Medicine B, Zerifin, Israel.
  • Agmon-Levin N; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Sheba Medical Center, Center for Autoimmune Diseases, Clinical Immunology, Angioedema and Allergy Unit, Tel-Hashomer, Israel.
  • Koren-Michowitz M; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Shamir Medical Center, Department of Hematology, Zerifin, Israel.
  • Amit-Vazina M; Shamir Medical Center, Internal Medicine B, Rheumatology Unit, Zerifin, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Eur J Rheumatol ; 9(4): 217-220, 2022 Oct.
Article em En | MEDLINE | ID: mdl-35943464
ABSTRACT
Macrophage activation syndrome is the most frequent life-threatening complication of adult-onset Still's disease. This is a nearly fatal case of a young patient, which has been refractory to corticoste- roids, anakinra, tocilizumab, cyclosporine A, and etoposide, but eventually responded miraculously to salvage therapy with ruxolitinib. We review recent pertinent data related to the therapeutic value of ruxolitinib for macrophage activation syndrome triggered by adult-onset Still's disease.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article