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作 者:杨钰 陈萍 叶宝英[1] 孙陶陶 牛建梅[1] 周雷平[1] 王慧[1] 施立晔[1] 陈炯[1] YANG Yu;CHEN Ping;YE Baoying;SUN Taotao;NIU Jianmei;ZHOU Leiping;WANG Hui;SHI Liye;CHEN Jiong(Department of Ultrasound,The International Peace Maternity and Child Health Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai Key Laboratory of Embryo Original Diseases,Shanghai 200030,China;Department of Radiology,The International Peace Maternity and Child Health Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai Key Laboratory of Embryo Original Diseases,Shanghai 200030,China)
机构地区:[1]上海交通大学医学院附属国际和平妇幼保健院超声科,上海市胚胎源性疾病重点实验室,上海200030 [2]上海交通大学医学院附属国际和平妇幼保健院放射科,上海市胚胎源性疾病重点实验室,上海200030
出 处:《肿瘤影像学》2024年第2期174-179,共6页Oncoradiology
基 金:上海市卫生健康委员会卫生行业临床研究专项(202340010)。
摘 要:目的:探讨产前超声联合磁共振成像(magnetic resonance imaging,MRI)对胎儿心脏横纹肌瘤(cardiac rhabdomyoma,CR)及结节性硬化症(tuberous sclerosis complex,TSC)的诊断价值。方法:回顾并分析2010年1月—2022年10月上海交通大学医学院附属国际和平妇幼保健院经产前超声诊断及疑似胎儿CR的临床资料和影像学特征。结果:经产前超声检查共诊断或疑似胎儿CR 41例,均为单胎。同时行MRI检查者30例(73.2%),其中11例诊断为单纯性CR(36.7%),16例(53.3%)CR合并颅内TSC,3例MRI未发现胎儿心脏占位性病变,其中1例出生后心脏超声证实为肥大肌束,1例新生儿心脏超声检查正常,1例失访。41例中12例在产前进一步行染色体核型分析及全外显子组测序(whole exome sequencing,WES),4例发现异常,3例基因检测证实TSC基因突变。结论:产前超声是CR的首选检查方法,对CR的检出及诊断具有重要价值。而超声联合MRI可进一步提高CR的诊断准确度和TSC检出率,结合染色体核型及TSC相关基因检测,可更好地提供产前诊断咨询及预后评估。Objective:To investigate the diagnostic value of prenatal ultrasound combined with magnetic resonance imaging(MRI)in fetal cardiac rhabdomyoma(CR)and tuberous sclerosis complex(TSC).Methods:Retrospectively analyzed the clinical data,ultrasound and MRI imaging features of prenatal ultrasound diagnosed and suspected fetal CR in The International Peace Maternity,Shanghai Jiao Tong University School of Medicine and Child Health Hospital from January 2010 to October 2022.Results:A total of 41 cases of fetal CR were diagnosed or suspected by prenatal ultrasonography,all of which were singletons.At the same time,30 cases(73.2%)underwent MRI examination,of which 11 cases(36.7%)were diagnosed as simple CR,16 cases(53.3%)were combined with intracranial TSC.At the same time,3 cases of MRI did not find fetal cardiac mass,of which 1 case was confirmed as hypertrophic muscle bundle by echocardiography after birth,1 case of neonatal echocardiography was normal,and 1 case was lost to follow-up.Among the 41 cases,12 cases underwent further prenatal karyotype analysis and whole exome sequencing(WES),4 cases were found to be abnormal,and 3 cases were confirmed to have TSC gene mutation by gene detection.Conclusion:Prenatal ultrasound is the first choice for CR,which is of great value in the detection and diagnosis of CR.Ultrasound combined with MRI can further improve the diagnostic accuracy of CR and the detection rate of TSC.Combined with chromosome karyotype and TSC related gene detection,it can provide better prenatal diagnosis consultation and prognosis evaluation.
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