Refractory macrophage activation syndrome in the setting of adult‐onset Still disease with hemophagocytic lymphohistiocytosis detected on skin biopsy treated with canakinumab and tacrolimus
Author:
Affiliation:
1. Department of DermatologyUT Southwestern Medical Center Dallas Texas
2. Department of Allergy and ImmunologyUT Southwestern Medical Center Dallas Texas
Publisher
Wiley
Subject
Dermatology,Histology,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cup.13466
Reference22 articles.
1. A comprehensive review on adult onset Still's disease
2. Preliminary criteria for classification of adult Still's disease;Yamaguchi M;J Rheumatol,1992
3. Persistent pruritic papules and plaques: a characteristic histopathologic presentation seen in a subset of patients with adult-onset and juvenile Still's disease
4. Clinical characteristics and follow-up analysis of adult-onset Still’s disease complicated by hemophagocytic lymphohistiocytosis
5. Macrophage Activation Syndrome in Patients Affected by Adult-onset Still Disease: Analysis of Survival Rates and Predictive Factors in the Gruppo Italiano di Ricerca in Reumatologia Clinica e Sperimentale Cohort
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3. Young Woman With Annular and Purpuric Plaques in the Setting of High Fevers: Answer;The American Journal of Dermatopathology;2023-05
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