Castro Leonor, Ferreira Ana C, Cohen Álvaro, Macedo Israel J, Tomé Teresa
Pediatric and Neonatal Intensive Care Unit, Hospital Central do Funchal, Av. Luís de Camões, nº 57 - 9004-514 Funchal, Madeira, Portugal.
Metabolic Diseases Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário de Lisboa Central, Lisboa, Portugal.
Case Rep Perinat Med. 2022 Feb 1;11(1):20210083. doi: 10.1515/crpm-2021-0083. eCollection 2022 Jan.
Pearson syndrome is a mitochondrial cytopathy with multisystemic involvement that typically presents in infancy and has poor prognosis. We aim to present a case that is distinct due to the timing of presentation and associated anomalies.
We report the case of preterm monochorionic twins with transfusion dependent fetal anemia that had post-natal multisystem dysfunction which led to the diagnosis of Pearson syndrome.
This case highlights the possibility of antenatal presentation of Pearson syndrome, which should be considered in cases of severe fetal anemia without an apparent cause.
皮尔逊综合征是一种累及多系统的线粒体细胞病,通常在婴儿期发病,预后较差。我们旨在报告一例因发病时间和相关异常而具有独特性的病例。
我们报告了一对早产单绒毛膜双胎的病例,他们患有输血依赖型胎儿贫血,出生后出现多系统功能障碍,最终诊断为皮尔逊综合征。
该病例突出了皮尔逊综合征产前发病的可能性,在病因不明的严重胎儿贫血病例中应予以考虑。