Prenatal Diagnosis of Bilateral Meromelia Coexisting With Duodenal Atresia: Case Report of a Rare Anomalous Combination With Three-Dimensional Sonography

Ameen Muftiat Omolola, Awowole Ibraheem Olayemi, Abdur-Rahim Zainab Foyeke, Muhammad-Olodo Abdulmujeeb Opeyemi
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Abstract

A rare case of bilateral fetal meromelia with duodenal atresia (DA) was diagnosed on three-dimensional (3D) sonography. A 32-year-old G3P2002 with a large for date uterus, was reviewed at 26 weeks’ gestation. The 3D sonogram confirmed the presence of the humerus, olecranon process, and only the proximal third of the ulna bone, bilaterally. The distal ulna, radius, metacarpals, and phalanges were absent on both upper limbs. The bones of the lower limbs were present and appropriate for gestational age. Further evaluation revealed the “double bubble” sign, which is characteristic of DA within the fetal abdomen. The patient was induced 2 weeks later, due to intrauterine fetal demise. The suspected fetal anomalies were confirmed at birth. A high index of suspicion and a detailed sonographic evaluation are essential for detecting rare fetal anomalies, such as meromelia.
产前诊断双侧子午畸形与十二指肠闭锁并存:利用三维超声诊断罕见异常组合的病例报告
通过三维(3D)超声诊断出一例罕见的双侧胎儿绒毛膜膨出伴十二指肠闭锁(DA)病例。一名 32 岁的 G3P2002 孕妇在妊娠 26 周时接受了检查,其子宫较大。三维声像图证实双侧肱骨、肩胛骨突和尺桡骨近端三分之一的骨骼存在。双上肢没有尺骨远端、桡骨、掌骨和趾骨。下肢骨存在,且与胎龄相符。进一步评估发现了 "双气泡 "征,这是胎儿腹腔内DA的特征。由于胎儿宫内死亡,患者在两周后接受了引产手术。怀疑的胎儿畸形在出生时得到证实。高度的怀疑指数和详细的超声评估对于发现胎儿罕见畸形(如子宫腔畸形)至关重要。
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