Yada Kunpalin, Elka Miller, Ingrid Larsen, Kamini Raghuram, Catherine Windrim, Nimrah Abbasi, Greg Ryan, Tim Van Mieghem, Shiri Shinar
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引用次数: 0
Abstract
Introduction: Severe brain injury has been reported following fetoscopic laser ablation (FLA) for twin-to-twin transfusion syndrome (TTTS), but imaging patterns and temporal evolution remain poorly defined. This study aimed to characterize the progression of severe brain injury after FLA.
Methods: We conducted a retrospective case series of TTTS pregnancies with severe brain injury identified after FLA at the Ontario Fetal Center (June 2023-March 2025). FLA was performed for Quintero stage ≥ II and selected stage I cases. Severe abnormalities were defined as severe intraventricular haemorrhage or destructive lesions. Serial ultrasound and fetal MRI were reviewed and categorized as early (< 4 weeks) or late (≥ 4 weeks) post-FLA.
Results: Fifteen fetuses from 14 pregnancies were identified. Mean gestational age at FLA was 19.7 ± 3.2 weeks; 66.7% were stage III-IV and 60% were donor twins. Early imaging (n = 8) most commonly showed periventricular haemorrhagic infarction (62.5%) and cerebellar haemorrhage (25.0%). Late imaging (n = 13) predominantly demonstrated cerebral volume loss (76.9%), often involving the parietal lobes, with polymicrogyria (38.5%) and Wallerian degeneration (30.8%). Findings remained unchanged after 4 weeks.
Conclusion: Brain injury after FLA evolves from acute haemorrhagic/ischaemic insults to irreversible destructive changes. These preliminary findings suggest a consistent pattern of injury that warrants further prospective study.
期刊介绍:
Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling