Prenatally diagnosed case of tricuspid valve dysplasia: A case report with review of the literature

被引:1
作者
Agarwal, Prateek [1 ]
Agarwal, Rajesh [2 ]
机构
[1] Kempegowda Inst Med Sci, Dept Radiodiag, Bengaluru, Karnataka, India
[2] Meera Hosp, Dept Ultrasound, Shiv Marg,Bani Pk, Jaipur, Rajasthan, India
关键词
Dysplasia; non-immune hydrops; pulmonary atresia; tricuspid annulus; tricuspid regurgitation; tricuspid valve; PULMONARY-ARTERY SIZE; FETAL LUNG-VOLUMES; FETUS; HEART; SPECTRUM; ATRESIA;
D O I
10.4103/ijri.IJRI_463_18
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We present a case of fetal tricuspid valve dysplasia (TVD) and pulmonary atresia, diagnosed during a routine obstetric ultrasound scan. Serial fetal echocardiographic evaluations revealed progressively augmented prodigious thickening of the tricuspid valvular and subvalvular structures, which eventually extensively obliterated the right ventricle cavity. Thickened dysplastic valve displayed a "cotton-wool" appearance. Unusual configurations of three vessels in the three-vessel view were also observed on a consecutive gray scale and color Doppler scans. During pregnancy, the fetus exhibited satisfactory growth parameters, and complications of progressive hemodynamic compromise associated with TVD and pulmonary atresia such as grievous hydrops or arrhythmia did not develop till 39 weeks of gravidity.
引用
收藏
页码:452 / 456
页数:5
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