A case of hereditary alpha tryptasemia and presumptive eosinophilic granulomatosis with polyangiitis

Sonia Iqbal*, Joseph A. Baxter, Karla E. Adams

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

This case is notable for the potential overlap of hereditary alpha tryptasemia and eosinophilic granulomatosis with polyangiitis. The successful use of mepolizumab, initially for eosinophilic granulomatosis with polyangiitis but potentially benefiting the patient's hereditary alpha tryptasemia, offers a novel approach to managing complex cases involving both rare disorders.

Original languageEnglish
Article number100481
JournalJournal of Allergy and Clinical Immunology: Global
Volume4
Issue number3
DOIs
StatePublished - Aug 2025

Keywords

  • elevated tryptase level
  • eosinophilic granulomatosis with polyangiitis
  • Hereditary alpha tryptasemia
  • hypereosinophilia
  • mepolizumab

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