Gan YuanZhu, Wang HuiJuan, Zheng Zebing, Tang Chengyan, Zhu Daiwei, Xia Xingrong, Huang Lu, Du Qing, Liao XiLin, Liu Yuanmei, Jin Zhu
Department of Pediatric Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, 563003, China.
Department of Pediatric Surgery, Guizhou Children Hospital, Zunyi, 563003, China.
BMC Pediatr. 2025 May 22;25(1):411. doi: 10.1186/s12887-025-05740-3.
We present a rare case of a 3-day-old male infant presenting with both annular pancreas (AP) and H-type esophageal atresia (H-TEF). Initially, our focus was solely on the upper gastrointestinal malformation in the child, and the misdiagnosis of a concurrent Tracheoesophageal fistula (TEF) was corrected only after a secondary surgery. Therefore, this article aims to discuss methods for accurately diagnosing this rare anomaly and performing timely surgery to improve the prognosis of the child and enhance their quality of life.
我们报告了一例罕见的3日龄男婴，同时患有环状胰腺（AP）和H型食管闭锁（H-TEF）。最初，我们仅关注患儿的上消化道畸形，且仅在二次手术后才纠正了并发气管食管瘘（TEF）的误诊。因此，本文旨在探讨准确诊断这种罕见异常并及时进行手术的方法，以改善患儿预后并提高其生活质量。
