Pulmonary interstitial glycogenosis in identical twins

Pediatr Pulmonol. 2005 Oct;40(4):362-6. doi: 10.1002/ppul.20255.

Abstract

We present the clinical, radiological, and pathological findings of open lung biopsies from monozygotic prematurely born male twins with respiratory distress at ages 6 and 8 weeks postnatally. Radiological examination showed a reticular nodular interstitial pattern on chest radiography. High-resolution computed tomography (HRCT) revealed ground-glass opacification and thickened interstitial septae in both infants. Lung biopsies showed a similar histology. There was diffuse interstitial thickening of the alveolar septa by mesenchymal cells, without prominent hyperplasia of type 2 pneumocytes, and without airspace exudates. Sections were periodic acid-Schiff (PAS)-positive within the cytoplasm of interstitial cells, indicating the presence of glycogen. Thus the diagnosis of pulmonary interstitial glycogenosis was made. Both infants were treated with glucocorticoids and had a favorable outcome. We speculate that pulmonary interstitial glycogenosis could be a histopathological form of chronic lung disease (CLD) of infancy.

Publication types

  • Case Reports
  • Twin Study

MeSH terms

  • Diseases in Twins
  • Glycogen Storage Disease / diagnostic imaging*
  • Glycogen Storage Disease / pathology
  • Humans
  • Infant
  • Lung Diseases / diagnostic imaging*
  • Lung Diseases / pathology
  • Male
  • Radiography
  • Twins, Monozygotic