Progressive Restrictive Ventilatory Impairment in Idiopathic Diffuse Pulmonary Ossification

Intern Med. 2018 Jun 1;57(11):1631-1636. doi: 10.2169/internalmedicine.9433-17. Epub 2018 Jan 11.

Abstract

Diffuse pulmonary ossification (DPO) is a rare disease characterized by metaplastic bone formation in the lung. There are few reports with a long-term follow-up of this disease. We herein report a 47-year-old man diagnosed with idiopathic DPO at 30 years of age. The patient's vital capacity was normal until 36 years of age (3.39 L, 82.4% predicted), but it was severely decreased when he visited the hospital again at 47 years of age due to cough and dyspnea (1.98 L, 44.6% predicted). Chest computed tomography showed a significant increase in the number of high-density nodules, suggesting that the progression of DPO had caused restrictive ventilatory impairment.

Keywords: prognosis; pulmonary ossification; restrictive ventilatory impairment.

Publication types

  • Case Reports

MeSH terms

  • Cough / etiology
  • Disease Progression
  • Humans
  • Lung Diseases, Interstitial / complications
  • Lung Diseases, Interstitial / diagnosis*
  • Lung Diseases, Interstitial / physiopathology
  • Male
  • Middle Aged
  • Ossification, Heterotopic
  • Rare Diseases
  • Tomography, X-Ray Computed
  • Vital Capacity