Hematopoietic stem cell transplantation for pulmonary alveolar proteinosis associated with primary immunodeficiency disease

被引:0
作者
Mari Tanaka-Kubota
Koji Shinozaki
Satoshi Miyamoto
Masakatsu Yanagimachi
Tsubasa Okano
Noriko Mitsuiki
Masahiro Ueki
Masafumi Yamada
Kohsuke Imai
Masatoshi Takagi
Kazunaga Agematsu
Hirokazu Kanegane
Tomohiro Morio
机构
[1] Tokyo Medical and Dental University (TMDU),Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences
[2] Shinshu University,Department of Pediatrics, School of Medicine
[3] Hokkaido University Graduate School of Medicine,Department of Pediatrics
[4] Tokyo Medical and Dental University (TMDU),Department of Community Pediatrics, Perinatal and Maternal Medicine, Graduate School of Medical and Dental Sciences
[5] Shinshu University,Department of Infection and Host Defense, Graduate School of Medicine
来源
International Journal of Hematology | 2018年 / 107卷
关键词
Pulmonary alveolar proteinosis; Hematopoietic stem cell transplantation; Primary immunodeficiency; Granulocyte–macrophage colony stimulating factor; Bronchoalveolar lavage;
D O I
暂无
中图分类号
学科分类号
摘要
Pulmonary alveolar proteinosis (PAP) is a rare disorder that is characterized by the excessive accumulation of surfactant-like materials in the alveoli, leading to hypoxemic respiratory failure. We describe two Japanese infants with PAP associated with hypogammaglobulinemia and monocytopenia. These patients may have underlying primary immunodeficiency (PID) and were successfully treated with allogeneic hematopoietic stem cell transplantation (HSCT). This report indicates that allogeneic HSCT may provide a curative treatment for PAP associated with PID.
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页码:610 / 614
页数:4
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