Cough in hypereosinophilic syndrome: case report and literature review

BMC Pulm Med. 2020 Apr 15;20(1):90. doi: 10.1186/s12890-020-1134-x.

Abstract

Background: Cough and airway eosinophilic inflammation has not been highlighted in hypereosinophilic syndrome (HES).

Case presentation: We report 2 further cases and reviewed the clinical features and treatment of HES present with cough from the literature. Both cases were middle age male, presenting with chronic cough, airway eosinophilic inflammation and hyper eosinophilia who have been previous misdiagnosed as cough-variant asthma and failed anti-asthma treatment. PDGFRA fusion gene was confirmed in one case, but not in the other case. Both had evidence of myeloproliferative features. The tyrosine kinase inhibitor, imatinib, resulted in complete resolution of eosinophilia and cough. By searching PubMed, we found 8 HES cohorts of 411 cases between 1975 and 2013, where the incidence of cough was 23.11%. Sixteen case reports of HES presented with cough as predominant or sole symptom, with nine male patients with positive PDGFRA fusion gene, who responded well to imatinib. Six of seven patients, who tested negative for the PDGFRA, responded to systemic glucocorticoids.

Conclusions: Cough and airway eosinophilic inflammation is common in some HES patients. PDGFRA+ HES patients present with chronic cough respond well to imatinib. Our case reports indicate that PDGFRA negative HES patients may respond to imatinib as well.

Keywords: Airway eosinophilic inflammation; Cough; Hypereosinophilic syndrome; Imatinib; PDGFRA fusion gene.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Cough / drug therapy
  • Cough / etiology*
  • Humans
  • Hypereosinophilic Syndrome / diagnosis*
  • Hypereosinophilic Syndrome / drug therapy
  • Hypereosinophilic Syndrome / genetics
  • Imatinib Mesylate / therapeutic use*
  • Male
  • Middle Aged
  • Oncogene Proteins, Fusion / genetics
  • Protein Kinase Inhibitors / therapeutic use*
  • Tomography, X-Ray Computed

Substances

  • Oncogene Proteins, Fusion
  • Protein Kinase Inhibitors
  • Imatinib Mesylate