Pulmonary Alveolar Proteinosis with Bilateral Ground-glass Opacities Localized in Subpleural Areas

  • Mohri Keiji
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Miyashita Naoyuki
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Obase Yasushi
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Fukuda Minoru
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Ohue Yoshihiro
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Ueno Shiro
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Yagi Shin-ichi
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Yoshida Koichiro
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Kobashi Yoshihiro
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School
  • Soda Hiroshi
    Second Department of Internal Medicine, Nagasaki University Hospital
  • Oka Mikio
    Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School

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Abstract

Background. Pulmonary alveolar proteinosis (PAP) located only in subpleural areas is quite rare. Case. A 32-year-old asymptomatic nonsmoker woman was found to have bilateral ground-glass opacities in subpleural areas from basal to apical segments. The bronchoalveolar lavage fluid had a light-milky appearance and contained large eosinophilic bodies stained with periodic acid-Schiff. Anti-GM-CSF antibody in the serum and the lavage fluid was markedly elevated to 632μg/ml and 1.4μg/ml, respectively. These findings were consistent with acquired PAP. The opacities partly improved spontaneously during 15 months. Conclusion. Ground-glass opacities localized in subpleural areas are rare in alveolar proteinosis, however, detailed analysis of lavage fluid should be actively done for diagnosis.

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