Chronic myelomonocytic leukemia-associated pulmonary alveolar proteinosis: A case report and review of literature

被引:1
|
作者
Can Chen [1 ]
Xi-Lian Huang [1 ]
Da-Quan Gao [1 ]
Yi-Wei Li [2 ]
Shen-Xian Qian [1 ]
机构
[1] Department of Hematology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine
[2] Department of Intensive Care Unit, Affiliated Hangzhou First People’s Hospital,Zhejiang University School of Medicine
关键词
D O I
暂无
中图分类号
R733.72 [慢性白血病]; R563 [肺疾病];
学科分类号
1002 ; 100201 ; 100214 ;
摘要
BACKGROUND Pulmonary alveolar proteinosis(PAP) is a rare condition that can cause progressive symptoms including dyspnea, cough and respiratory insufficiency.Secondary PAP is generally associated with hematological malignancies including chronic myelomonocytic leukemia(CMML).To the best of our knowledge, this is the first reported case of PAP occurring secondary to CMML.CASE SUMMARY We report the case of a 63-year-old male who presented with a recurrent cough and gradually progressive dyspnea in the absence of fever.Based upon clinical symptoms, computed tomography findings, bone marrow aspiration, flow cytometry studies and cytogenetic analyses, the patient was diagnosed with PAP secondary to CMML.He underwent whole lung lavage in March 2016 to alleviate his dyspnea, after which he began combined chemotherapeutic treatment with decitabine and cytarabine.The patient died in January 2020 as a consequence of severe pulmonary infection.CONCLUSION This case offers insight regarding the mechanistic basis for PAP secondary to CMML and highlights potential risk factors.
引用
收藏
页码:1156 / 1167
页数:12
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