Respiratory Medicine Case Reports (Jan 2023)

A case of development of autoimmune pulmonary alveolar proteinosis during the treatment of hypersensitivity pneumonitis

  • Maki Asami-Noyama,
  • Kosuke Ito,
  • Misa Harada,
  • Yukari Hisamoto,
  • Yoshie Kunihiro,
  • Eiji Ikeda,
  • Tasuku Yamamoto,
  • Junki Suizu,
  • Ayumi Fukatsu,
  • Syuichiro Ohata,
  • Yoriyuki Murata,
  • Keiji Oishi,
  • Yoshikazu Yamaji,
  • Nobutaka Edakuni,
  • Tomoyuki Kakugawa,
  • Tsunahiko Hirano,
  • Kazuto Matsunaga

Journal volume & issue
Vol. 44
p. 101862

Abstract

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Herein, we report the case of a 73-year-old woman with an occupational history of plaster grinding who developed autoimmune pulmonary alveolar proteinosis (PAP) during the treatment of fibrotic hypersensitivity pneumonitis with steroids and immunosuppressive drugs. Based on the changes in computed tomography imaging findings, poor response to steroid therapy, and markedly elevated KL-6 levels, PAP was suspected and diagnosed by bronchoscopy. Repeated segmental bronchoalveolar lavage under high-flow nasal cannula oxygen therapy resulted in slight improvement. Steroids and immunosuppressive treatments for other interstitial lung diseases may cause PAP or exacerbate latent PAP.

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