Goff Ryan D, Soares Bruno P
1 Inland Imaging, Washington, USA.
2 Russell H Morgan Department of Radiology and Radiological Science, The Johns Hopkins Hospital, USA.
Neuroradiol J. 2018 Aug;31(4):412-414. doi: 10.1177/1971400916689575. Epub 2017 Feb 14.
Patau syndrome remains a difficult diagnosis for parents and a challenging conversation for clinicians due to the overall poor prognosis. Previous population-based reports have documented the sobering life expectancies of these patients, with few surviving to 1 year of age. Despite the high mortality rate in infants born with trisomy 13, there are several reports of survival into late childhood and early adulthood. While clinical outcomes have been well documented, there has been a paucity of literature describing postnatal imaging findings in long-term survivors. We present a case report of a 2-year-old girl with trisomy 13 who underwent brain magnetic resonance imaging examination at our institution to evaluate for possible structural abnormalities contributing to central sleep apnea. We describe the clinical and postnatal neuroimaging findings of this rare patient with trisomy 13. Understanding the spectrum of neuroradiological findings in long-term survivors with trisomy 13, in combination with other organ system abnormalities, could add important clinical information and help better predict patient outcomes and expectations among parents.
由于总体预后较差,帕陶综合征对父母来说仍然是一个难以诊断的疾病,对临床医生来说也是一次具有挑战性的谈话。以前基于人群的报告记录了这些患者令人清醒的预期寿命,很少有人能活到1岁。尽管13三体综合征患儿的死亡率很高,但仍有几例存活至儿童晚期和成年早期的报告。虽然临床结果已有充分记录,但描述长期存活者产后影像学表现的文献却很少。我们报告一例2岁13三体综合征女孩的病例,她在我们机构接受了脑磁共振成像检查,以评估可能导致中枢性睡眠呼吸暂停的结构异常。我们描述了这位罕见的13三体综合征患者的临床和产后神经影像学表现。了解13三体综合征长期存活者的神经放射学表现谱,结合其他器官系统异常情况,可为临床提供重要信息,有助于更好地预测患者预后,并帮助家长更好地预期。