Macrophage Activation Syndrome in Children: Update on Diagnosis and Treatment.

children diagnosis macrophage activation syndrome review treatment

Journal

Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936

Informations de publication

Date de publication:
21 Jun 2024
Historique:
received: 30 05 2024
revised: 18 06 2024
accepted: 20 06 2024
medline: 27 7 2024
pubmed: 27 7 2024
entrez: 27 7 2024
Statut: epublish

Résumé

Macrophage activation syndrome (MAS) is potentially fatal; so, early diagnosis and timely treatment are essential. However, detecting MAS is sometimes challenging because its principal features can be observed in other pediatric diseases that cause severe inflammation. Cytokine storm due to immune dysregulation represents the clinical and laboratory features of MAS that are included in the diagnostic criteria. Most cases of MAS occur as an underlying condition worsens and progresses. Therefore, a patient with autoimmune or autoinflammatory disease who shows unexplained clinical deterioration despite appropriate management should be considered at high risk for MAS (i.e., occult MAS). The basic principles of treatment are control of triggering factors, supportive care, and relief of hyperinflammation. Systemic steroids and cyclosporine A are frequently used as a first-line treatment. For the treatment of refractory MAS, cytokine-specific biologic agents such as anakinra have recently become preferred over traditional immunosuppressive agents such as etoposide. MAS might be underrecognized in pediatric patients with infectious and inflammatory diseases due to its diverse clinical presentations. Clinical suspicion of MAS is of the utmost importance for early recognition of the disease.

Identifiants

pubmed: 39062205
pii: children11070755
doi: 10.3390/children11070755
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Bucheon St. Mary's Hospital
ID : Institute of Clinical Medicine Research Fund, 2024.

Auteurs

Jin Lee (J)

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Department of Pediatrics, Incheon St. Mary's Hospital, The Catholic University of Korea, Incheon 21431, Republic of Korea.

Kil Seong Bae (KS)

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Department of Pediatrics, Eunpyeong St. Mary's Hospital, The Catholic University of Korea, Seoul 03312, Republic of Korea.

Jung Woo Rhim (JW)

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Department of Pediatrics, Daejeon St. Mary's Hospital, The Catholic University of Korea, Daejeon 34943, Republic of Korea.

Soo-Young Lee (SY)

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Department of Pediatrics, Bucheon St. Mary's Hospital, The Catholic University of Korea, Bucheon 14647, Republic of Korea.
The Vaccine Bio Research Institute, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

Dae Chul Jeong (DC)

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
The Vaccine Bio Research Institute, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Department of Pediatrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.

Jin Han Kang (JH)

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
The Vaccine Bio Research Institute, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

Classifications MeSH