Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome

J Clin Immunol. 2013 Jul;33(5):896-902. doi: 10.1007/s10875-013-9890-5. Epub 2013 Apr 13.

Abstract

Purpose: Autosomal dominant hyper-IgE syndrome (AD-HIES) due to heterozygous STAT3 mutation is a primary immunodeficiency characterized by eczema, elevated serum IgE, recurrent infections, and connective tissue and skeletal findings. Healing of pneumonias is often abnormal with formation of pneumatoceles and bronchiectasis. We aimed to explore whether healing after lung surgery is also aberrant.

Methods: We retrospectively analyzed the medical records of 32 patients with AD-HIES who received lung surgery for the management of pulmonary infections from 1960 to 2011. We collected information including patient demographics, STAT3 mutation status, clinical history, surgical and medical procedures performed, complications, related medical treatments, and outcomes.

Results: More than 50% of lung surgeries had associated complications, with the majority being prolonged bronchopleural fistulae. These fistulae often led to empyemas that necessitated additional interventions including prolonged antibiotics, prolonged thoracostomy tube drainage and re-operations.

Conclusion: Lung surgery in AD-HIES patients is associated with high complication rates. STAT3 mutations likely lead to abnormalities in tissue remodelling that are further exacerbated by infection.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Job Syndrome / immunology*
  • Job Syndrome / physiopathology*
  • Lung / immunology
  • Lung / physiopathology
  • Lung / surgery
  • Lung Diseases / genetics
  • Lung Diseases / immunology
  • Lung Diseases / physiopathology*
  • Lung Diseases / surgery*
  • Male
  • Middle Aged
  • Mutation
  • Retrospective Studies
  • STAT3 Transcription Factor / genetics
  • Wound Healing / genetics
  • Wound Healing / physiology*
  • Young Adult

Substances

  • STAT3 Transcription Factor
  • STAT3 protein, human