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从双胎贫血-红细胞增多序列征迅速转变为双胎输血综合征

Rapid Change From Spontaneous Twin Anemia Polycythemia Sequence to Twin-to-Twin Transfusion Syndrome.

作者信息

Horie Kenji, Ozawa Katsusuke, Okusa Takafumi, Sugibayashi Rika, Wada Seiji, Takahashi Hironori

机构信息

Department of Obstetrics and Gynecology, Jichi Medical University, Shimotsuke, JPN.

Center for Maternal-Fetal, Neonatal and Reproductive Medicine, National Center for Child Health and Development, Tokyo, JPN.

出版信息

Cureus. 2025 Apr 2;17(4):e81608. doi: 10.7759/cureus.81608. eCollection 2025 Apr.

Abstract

A new natural course of spontaneous twin anemia polycythemia sequence (TAPS) was clarified. A 29-year-old woman, who conceived monochorionic diamniotic twins, showed elevation of the peak systolic velocity of the middle cerebral artery (MCA-PSV) in one twin at 24+2 weeks. The other twin showed a decrease in MCA-PSV. The amniotic volume did not differ between the twins. We diagnosed them with TAPS. Four days later, maximum vertical pockets were 19 and 97 mm in the donor and recipient, respectively. We diagnosed them with twin-twin transfusion syndrome, Quintero stage 1. Fetoscopic laser photocoagulation was employed, and the post-operative course was uneventful. Emergent cesarean section was conducted at 33+0 weeks because of premature rupture of the membranes. Neither twin showed anemia nor polycythemia. Only one patient with spontaneous TAPS followed by twin-to-twin transfusion syndrome (TTTS) has been reported so far. To our knowledge, this is the first report of a pregnant woman with TAPS developing TTTS within a few days.

摘要

明确了一种新的自然发生的双胎贫血-红细胞增多序列征(TAPS)病程。一名29岁的孕妇怀有单绒毛膜双羊膜囊双胎,在孕24⁺²周时,其中一个胎儿的大脑中动脉收缩期峰值速度(MCA-PSV)升高,另一个胎儿的MCA-PSV降低。两个胎儿的羊水量无差异。我们诊断她们患有TAPS。四天后,供血儿和受血儿的最大羊水深度分别为19和97毫米。我们诊断她们患有双胎输血综合征,Quintero 1期。采用了胎儿镜激光凝固术,术后过程顺利。因胎膜早破,在孕33⁺⁰周时进行了急诊剖宫产。两个胎儿均未出现贫血或红细胞增多。迄今为止,仅报道过1例自发TAPS随后发展为双胎输血综合征(TTTS)的患者。据我们所知,这是首例TAPS孕妇在数天内发展为TTTS的报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4df9/12047672/ee743f644866/cureus-0017-00000081608-i01.jpg

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