Utility of the sonographic syndromic pattern approach in diagnosis of aneuploidy in a low resource setting: case report

C. Verenga, S. Farayi, L. Hlatshwayo, AS Zanga, M. Ndagurwa, M. Nkomo, F. Rupande, ML Khumbula
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Abstract

Background: Aneuploidies pose a diagnostic challenge in low resource settings where diagnostic tests are unavailable or costs are beyond the reach of many. This provides a clinical challenge in case management and counselling for women with foetuses carrying multiple congenital anomalies. A pragmatic approach in the management of foetal medicine cases in these settings becomes imperative. Design: Screening survey and diagnostic test, the well accepted standard for Aneuploidy screen and laboratory tests. In this case we seek to illustrate the use of ultrasound in low resource setting where diagnostic tests are expensive and inaccessible. Setting: This was a hospital-bases case in a low-income setting. Subjects: A 45-year-old woman in her first pregnancy was referred at 20 weeks gestation to the Fetal Medicine Unit (FMU) with an ultrasound scan diagnosis of exomphalos. Intervention: A syndromic pattern approach was used in making a clinical diagnosis of trisomy 18 in a setting with ultrasound equipment and well-trained personnel. The syndromic pattern approach recognises that the common aneuploids such as Trisomy 21, 18 and 13, Monosomy X and Triploidy have a set of foetal malformations that accompany each of the syndromes. Main Outcome Measures: Diagnosis of Aneuploidy Results: A large exomphalos containing bowel and liver was identified. Additional abnormalities were identified which included bilateral mild ventriculomegaly, choroid plexus cysts, left diaphragmatic hernia, atrioventricular septal defect, and kyphoscoliosis of the thoracolumbar vertebrae. Conclusion: The case illustrates the utility of the sonographic syndrome approach in managing pregnancy with multiple foetal defects in low-resource settings. Core Tip: Aneuploidies pose a diagnostic challenge in low resource settings where diagnostic tests are unavailable or costs are beyond the reach of many. We report a case in which a sonographic syndromic pattern approach was used in making a clinical diagnosis of trisomy 18 in a setting with ultrasound equipment and well-trained personnel. This approach helps with case management and patient counselling.
超声综合征模式方法在低资源环境下诊断非整倍体的应用:病例报告
背景:非整倍体在资源匮乏的环境中构成了诊断挑战,在这些环境中,诊断测试不可用或成本超出了许多人的承受能力。这为胎儿携带多种先天性畸形的妇女的病例管理和咨询提供了临床挑战。在这些情况下,必须采取务实的方法来管理胎儿医学病例。设计:筛查调查和诊断测试,非整倍体筛查和实验室测试的公认标准。在这种情况下,我们试图说明超声在低资源环境中的使用,在这种环境中,诊断测试是昂贵且无法获得的。背景:这是一个低收入背景下的医院案例。受试者:一名45岁的第一次怀孕的妇女在怀孕20周时被转诊到胎儿医学室(FMU),超声扫描诊断为外生殖器。干预:在超声设备和训练有素的人员的环境中,采用综合征模式方法对18三体进行临床诊断。综合征模式方法认识到,常见的非整倍体,如21、18和13三体、X染色体单体和三倍体,每种综合征都伴随着一系列胎儿畸形。主要结果指标:非整倍体的诊断结果:鉴定出一个含有肠道和肝脏的大型外泌体。还发现了其他异常,包括双侧轻度脑室肥大、脉络丛囊肿、左侧膈疝、房室间隔缺损和胸腰椎后凸畸形。结论:该病例说明了超声综合征方法在低资源环境下处理多胎儿缺陷妊娠的实用性。核心提示:非整倍体在资源匮乏的环境中构成了诊断挑战,在这些环境中,诊断测试不可用或成本超出了许多人的承受能力。我们报告了一个病例,其中使用超声综合征模式方法在超声设备和训练有素的人员的环境中对18三体进行临床诊断。这种方法有助于病例管理和患者咨询。
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