Literature DB >> 33926277

Long-term follow-up and successful treatment of pulmonary alveolar proteinosis without hypercholesterolemia with statin therapy: a case report.

Shenyun Shi1, Rujia Wang2, Ling Chen2, Yan Li1, Yingwei Zhang1, Xiaoyan Xin3, Shangwen Yang3, Yihua Wang4, Yonglong Xiao1,2,5, Kaifeng Xu6.   

Abstract

Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by the accumulation of excessive surfactant lipids and proteins in alveolar macrophages and alveoli. Oral statin therapy is a novel treatment for PAP with hypercholesterolemia. However, this treatment has never been described in a patient without hypercholesterolemia. Here, we present a case of successful treatment with atorvastatin for a patient with possibly unclassified PAP without hypercholesterolemia who responded poorly to whole lung lavage therapy and inhaled granulocyte-macrophage colony-stimulating factor. After 18 months of atorvastatin treatment, the patient experienced improvements in dyspnea, radiographic abnormalities and pulmonary function. The present case study supports the feasibility of statin therapy for PAP regardless of the level of cholesterol.

Entities:  

Keywords:  Pulmonary alveolar proteinosis; cholesterol; granulocyte-macrophage colony-stimulating factor; hypercholesterolemia; statin; therapy

Year:  2021        PMID: 33926277     DOI: 10.1177/03000605211010046

Source DB:  PubMed          Journal:  J Int Med Res        ISSN: 0300-0605            Impact factor:   1.671


  1 in total

1.  A case of autoimmune pulmonary alveolar proteinosis with severe respiratory failure treated with segmental lung lavage and oral statin therapy.

Authors:  Tomotsugu Takano; Keisuke Takeda; Satoshi Nakamura; Genta Akiyama; Nobuhisa Ando; Masashi Komori
Journal:  Respir Med Case Rep       Date:  2022-06-06
  1 in total

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