Xiao Pingping, Dong Zhigao, Wang Qingqing, Su Junnan, Chen Yongquan, Lin Yiwan
Department of Hematology and Rheumatology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Front Oncol. 2024 Nov 26;14:1475036. doi: 10.3389/fonc.2024.1475036. eCollection 2024.
Interstitial lung disease (ILD) is a rare clinical presentation of primary myelofibrosis (PMF).
We report a case of ILD as the main manifestation on admission. A 58-year-old man was diagnosed with PMF owing to worsening anemia following treatment failure for conventional interstitial pneumonia.
Anemia and interstitial pneumonia both significantly improved following treatment with a Janus kinase 2 gene inhibitor. In this report, we discuss the possible mechanisms underlying PMF complicated with ILD.
间质性肺疾病(ILD)是原发性骨髓纤维化(PMF)的一种罕见临床表现。
我们报告一例以ILD为入院主要表现的病例。一名58岁男性因传统间质性肺炎治疗失败后贫血加重而被诊断为PMF。
使用Janus激酶2基因抑制剂治疗后,贫血和间质性肺炎均明显改善。在本报告中,我们讨论了PMF合并ILD的潜在机制。