Revista Alergia México (Nov 2019)

Mast cell activation syndrome. About a clinical case

  • Ricardo Cardona,
  • Maria Angélica Muñoz-Ávila,
  • Catalina Gómez-Henao,
  • Susana Diez-Zuluaga,
  • Kenny Mauricio Gálvez-Cárdenas

DOI
https://doi.org/10.29262/ram.v66i4.587
Journal volume & issue
Vol. 66, no. 4
pp. 504 – 509

Abstract

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Background: Monoclonal mast cell activation syndrome is included in mast cell activation disorders in which, after a diagnostic process, it is not possible to meet the required criteria for a diagnosis of systemic mastocytosis. Clinical case: A 73-year-old woman who presented two events of anaphylaxis 15 minutes after the intake of yucca; with a positive skin test, elevated tryptase, and mast cells with abnormal phenotype in the bone marrow biopsy, and without criteria for systemic mastocytosis. Conclusions: The diagnosis of monoclonal mast cell activation syndrome requires high clinical suspicion for patients with recurrent anaphylaxis and elevated tryptase, for whom joint management with hematology is essential.

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