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作 者:孙文佳 郑静[1] 周建娅[1] 周建英[1] SUN Wenjia;ZHENG Jing;ZHOU Jianya;ZHOU Jianying(Department of Respiratory Disease,the First Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310003,China)
机构地区:[1]浙江大学医学院附属第一医院呼吸内科,浙江杭州310003
出 处:《浙江大学学报(医学版)》2023年第5期583-587,共5页Journal of Zhejiang University(Medical Sciences)
基 金:浙江省呼吸系统疾病临床研究中心(2022E50005)。
摘 要:一例54岁不吸烟的女性患者因背部疼痛就诊,影像学检查提示右下肺肿块。肺部穿刺活检提示腺癌,正电子发射计算机断层显像(PET)/计算机断层扫描(CT)提示肿瘤全身骨转移,确诊为ⅣB期右下肺腺癌(cT4N2M1c)伴骨转移。免疫组织化学检测显示间变性淋巴瘤激酶(ALK)基因重排,二代测序结果提示EML4-ALK融合(E6:A20),同时伴CCDC148-ALK(C1:A20)、PKDCC-ALK(Pintergenic:A20)和VIT-ALK(V15:A20)融合。患者在接受阿来替尼治疗后第32周出现咳嗽和活动后胸闷,复查CT提示双侧弥漫性磨玻璃影,考虑阿来替尼相关的间质性肺疾病。患者在停止阿来替尼治疗并予皮质类固醇治疗后,临床症状和CT均逐渐改善,但原发性肺部病变增大。采用克唑替尼后,患者在25个月随访期间原发性肺部病变和间质性肺疾病均未复发。A 54-year-old,non-smoking woman was diagnosed as stageⅣB adenocarcinoma with widespread bone metastasis(cT4N2M1c)in the First Affiliated Hospital,Zhejiang University School of Medicine.Immunohistochemistry result showed the presence of anaplastic lymphoma kinase(ALK)gene rearrangement;next-generation sequencing(NGS)indicated EML4-ALK fusion(E6:A20)with concurrent CCDC148-ALK(C1:A20),PKDCC-ALK(Pintergenic:A20)and VIT-ALK(V15:A20)fusions.After 32 weeks of alectinib treatment,the patient complained cough and exertional chest distress but had no sign of infection.Computed tomography(CT)showed bilateral diffuse ground glass opacities,suggesting a diagnosis of alectinib-related interstitial lung disease(ILD).Following corticosteroid treatment and discontinuation of alectinib,clinical presentations and CT scan gradually improved,but the primary lung lesions enlarged during the regular follow-up.The administration of crizotinib was then initiated and the disease was stable for 25 months without recurrence of primary lung lesions and ILD.
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