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A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas

机译:胎儿骶骨心肌畸胎瘤诊断和治疗的临床分析

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Objective:The present study aims to discuss the clinical features, treatment, and prognosis of fetal sacrococcygeal teratomas (SCTs) to improve the standard of diagnosis and treatment.Methods:The clinical data of 15 pregnant females with fetal SCT, admitted to Fujian ?Maternity and Child Health Hospital from January 2013 to January 2020, were retrospectively analyzed with respect to clinical characteristics, imaging features, complications, treatment options, and pregnancy outcomes.Results:The 15 cases of fetal SCT were all detected by color ultrasonography. There were two cases of cystic tumors and 13 cases of solid cystic tumors. In terms of tumor blood supply, there was one case without blood flow signal, eight cases with little blood flow signal, and six cases with abundant blood flow. At the time of delivery, there were two cases with a tumor diameter less than 5 cm, five cases with a diameter of 5-10 cm, and eight cases with a diameter of more than 10 cm. In terms of tumor shape and location, there were two cases of type I, ten cases of type II, and three cases of type III. There were six cases with an increased fetal heart to chest ratio, four cases of fetal edema, three cases of placental edema, four cases of excessive amniotic fluid, one case of insufficient amniotic fluid, three cases of fetal distress, one case of stillbirth, two cases of gestational diabetes mellitus, two cases of mirror syndrome, and two cases of postpartum hemorrhage. According to the pathological diagnosis, there were seven cases of mature teratoma, seven cases of immature teratoma, and one case of mixed germ cell tumor. There were six cases of induced delivery, nine cases of cesarean section, one case of premature birth, and two cases of mild neonatal asphyxia.Conclusion:Fetal SCT was generally diagnosed by prenatal ultrasonography. The tumor blood supply, growth rate, size, nature of the tumor, clinical type, pathology, and maternal-fetal complications are all closely correlated with the prognosis. The timing and manner of the termination of pregnancy should be determined on the basis of the pregnant female, the fetus, and the tumor.? 2020 Zheng et al.
机译:目的:本研究旨在讨论胎儿骶骨心肌畸胎瘤(SCT)的临床特征,治疗和预后,以改善诊断和治疗的标准。方法:胎儿SCT的15名孕妇的临床资料,涉及福建?产妇和儿童保健医院从2013年1月到2020年1月,回顾性地分析了临床特征,成像特征,并发症,治疗方案和妊娠结局。结果:胎儿SCT的15例全部被彩色超声检查检测到。有两种囊性肿瘤和13例固体囊性肿瘤。在肿瘤血液供应方面,有一种情况下没有血流信号,血流信号少8例,血流丰富6例。在递送时,肿瘤直径小于5厘米,5例直径为5-10厘米的患者,直径为10厘米的8例。就肿瘤形状和位置而言,I型,II型病例的两种情况,以及三种型III型。有6例胎儿胎儿胸腺比例增加,胎儿水肿四个患者,胎盘水肿三种,羊水过量液体,羊水不足,胎儿窘迫三种情况,一个病房,一个病房两种妊娠期糖尿病患者,两种镜综合征病例,两种患者出血。根据病理诊断,有7例成熟畸胎瘤,7例未成熟畸胎瘤病例,以及一种混合生殖细胞瘤的情况。有6例诱导递送,9例剖宫产,一次过早出生的病例,以及两种温和新生儿窒息的病例。结论:胎儿SCT通常通过产前超声检查诊断。肿瘤血液供应,生长速度,尺寸,性质,临床类型,病理和母体胎儿并发症都与预后密切相关。应在怀孕的女性,胎儿和肿瘤的基础上确定妊娠期终止的时序和方式。 2020郑等人。

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