[Pulmonary fibrosis in Hermansky-Pudlak syndrome is not fully usual]

Ann Pathol. 2006 Dec;26(6):445-9. doi: 10.1016/s0242-6498(06)70753-2.
[Article in French]

Abstract

A 55-year-old female patient with Hermansky-Pudlak syndrome (albinism, thrombopathia and ceroid accumulation) underwent a single lung transplantation for pulmonary fibrosis. Examination of explanted lung showed usual interstitial pneumonia pattern associated with two unusual lesions: presence of numerous macrophages containing ceroid pigments within fibrosis and characteristic foamy swelling of pneumocytes. This later lesion, which has only been recently described, seems related to the mechanism of the disease by defect of surfactant secretion. This lesion allows the histological individualization of pulmonary fibrosis associated with Hermansky-Pudlak syndrome from idiopathic usual interstitial pneumonia.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Female
  • Hermanski-Pudlak Syndrome / complications*
  • Hermanski-Pudlak Syndrome / pathology*
  • Humans
  • Middle Aged
  • Pulmonary Fibrosis / etiology*
  • Pulmonary Fibrosis / pathology