Clinical features of macrophage activation syndrome as the onset manifestation of juvenile systemic lupus erythematosus
Author:
Affiliation:
1. Division of Infectious Diseases and Immunology
2. Division of Hematology/Oncology
3. Division of Nephrology
4. Division of Pathology, Saitama Children's Medical Center, Saitama, Japan
Publisher
Oxford University Press (OUP)
Subject
Rheumatology
Link
http://academic.oup.com/rheumap/advance-article-pdf/doi/10.1093/rap/rkz013/28639394/rkz013.pdf
Reference19 articles.
1. Macrophage activation syndrome;Ravelli;Hematol Oncol Clin North Am,2015
2. Hyperinflammation, rather than hemophagocytosis, is the common link between macrophage activation syndrome and hemophagocytic lymphohistiocytosis;Weaver;Curr Opin Rheumatol,2014
3. Macrophage activation syndrome: a severe and frequent manifestation of acute pancreatitis in 362 childhood-onset compared to 1830 adult-onset systemic lupus erythematosus patients;Gormezano;Semin Arthritis Rheum,2016
4. Features, treatment, and outcomes of macrophage activation syndrome in childhood-onset systemic lupus erythematosus;Borgia;Arthritis Rheumatol,2018
5. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis;Henter;Pediatr Blood Cancer,2007
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3. Life threatening macrophage activation syndrome as the initial presentation of systemic lupus erythematosus: A case report and review of the literature;The Egyptian Rheumatologist;2023-01
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