Atypical Twin-to-Twin transfusion syndrome case managed in a single centre in indonesia with fetoscopic laser photocoagulation and amniopatch: ‘Case Report’

D. Aldiansyah, B. Halim, S. Lumbanraja, E. M. Asroel, M. Fahdy, Hanudse Hartono, Thomson Thomson
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Abstract

The diagnostic criteria for Quintero staging in twin-to-twin transfusion syndrome (TTTS) are not applicable in all cases of TTTS, such as those in which the symptoms overlap with other monochorionic twin complications such as selective intrauterine growth restriction (sIUGR). A 25-year-old woman, G1P0A0, At 22-24 weeks’ gestational age was diagnosed with TTTS, with no outstanding history of medication use during pregnancy, and no family history of genetic disorder or twin pregnancy. In the donor twin, persistently absent end-diastolic flow in the umbilical artery was observed using Doppler velocimetry. Polyhydramnios was observed in the recipient twins. The fetal weight discordance between the twins was 39%. After two weeks of follow-up, we performed fetoscopic laser photocoagulation and successfully ablated five vascular anastomoses and amnioreduction by 2.5 liters. Five days after the laser surgery, the patient developed amniotic fluid leakage, and an amniopatch was performed. We did the caesarean section at 34 weeks because of severe preeclampsia, the donor and recipient birth weights were 1,120 g and 1,837 g, respectively (weight discordance 39%). The APGAR scores were 3/4 and 6/8, respectively. The donor twin died six days after delivery due to respiratory failure, and the recipient twin survived. Neonatal echocardiography of the surviving twin showed no tricuspid regurgitation. No long-term follow-up was performed. The traditional diagnostic criteria for TTTS stage 3 were not met and overlapped with the diagnostic criteria for sIUGR type 2. This is the first procedure reported in Indonesia for Atypical TTTS with the outcome, one twin survived. Some TTTS cases do not meet traditional diagnostic criteria and overlap with other monochorionic twin complications.
印度尼西亚一家中心通过胎儿镜激光光凝术和羊膜修补术治疗的非典型双胎输血综合征病例:"病例报告
双胎输血综合征(TTTS)的金特罗分期诊断标准并不适用于所有 TTTS 病例,例如症状与其他单绒毛膜双胎并发症重叠的病例,如选择性宫内生长受限(sIUGR)。 一名 25 岁的 G1P0A0 孕妇在孕 22-24 周时被诊断为 TTTS,她在怀孕期间没有明显的用药史,也没有家族遗传病史或双胎妊娠史。在供体双胎中,使用多普勒测速仪观察到脐动脉舒张末期血流持续缺失。受体双胎出现多胎妊娠。双胞胎之间的胎儿体重差异为 39%。随访两周后,我们进行了胎儿镜激光光凝术,成功消融了五处血管吻合口,羊水减少了2.5升。激光手术后五天,患者出现羊水渗漏,我们为其进行了羊膜修补术。由于重度子痫前期,我们在 34 周时进行了剖腹产,供体和受体的出生体重分别为 1,120 克和 1,837 克(体重不一致率为 39%)。APGAR评分分别为3/4和6/8。供体双胎在产后六天因呼吸衰竭死亡,受体双胎存活。存活双胎的新生儿超声心动图显示没有三尖瓣反流。没有进行长期随访。 该病例不符合 TTTS 第 3 期的传统诊断标准,与 sIUGR 第 2 型的诊断标准重叠。这是印度尼西亚报告的首例非典型 TTTS 手术,结果有一对双胞胎存活。 有些 TTTS 病例不符合传统诊断标准,并与其他单绒毛膜双胎并发症重叠。
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