Coexisting Remnants of the Omphalomesenteric Duct and Urachus in an Infant.

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2025-01-01 Epub Date: 2025-06-21 DOI:10.70352/scrj.cr.25-0003
Noboru Oyachi, Fuminori Numano
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Abstract

Introduction: Congenital anomalies of the umbilicus, including remnants of the omphalomesenteric duct and urachus, result from the incomplete regression of fetal structures around the 10th week of gestation. The coexistence of these anomalies in a single patient is exceptionally uncommon. This report presents the case of a neonate with an umbilical nodule and periumbilical cyst, subsequently identified as coexisting remnants of the omphalomesenteric duct and urachus.

Case presentation: This study reports the case of a 17-day-old female infant who presented with a small moist umbilical nodule and a persistent yellowish mucinous discharge. Initial treatment for umbilical granuloma failed to resolve the lesion. Imaging revealed a 2-cm cyst beneath the umbilicus and a cord-like structure connecting it to the bladder. Surgical exploration identified a 6-cm fibrous band extending from the cyst to the ileal wall, consistent with an omphalomesenteric duct remnant, and a 5-mm diameter urachal remnant connecting the cyst to the bladder. Histological analysis confirmed the presence of intestinal mucosa and transitional epithelium. The postoperative recovery of the patient was without complications.

Conclusions: This case elucidates the diagnostic challenges posed by persistent umbilical lesions and highlights the importance of detailed imaging and surgical exploration for identifying rare congenital anomalies. Histopathological confirmation is essential for an accurate diagnosis. Further research is required to clarify the embryological basis and clinical implications of these anomalies.

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婴儿脐肠管和尿管共存残余。
导语:胎儿结构在妊娠第10周左右不完全退化,导致脐部先天性异常,包括脐肠管和脐静脉的残余。在单个患者中同时出现这些异常是非常罕见的。本报告提出的情况下,新生儿脐结节和脐周囊肿,随后确定为共存残余的脐肠管和尿管内。病例介绍:本研究报告了一例17天大的女婴,其表现为小的湿润脐结节和持续的淡黄色粘液分泌物。脐带肉芽肿的初步治疗未能解决病变。成像显示脐下有一个2厘米的囊肿,并有一个将其连接到膀胱的索状结构。手术探查发现一条6厘米的纤维带从囊肿延伸到回肠壁,与残余的脐肠管一致,以及连接囊肿和膀胱的直径为5毫米的尿管残余。组织学分析证实存在肠黏膜和移行上皮。患者术后恢复无并发症。结论:本病例阐明了持续脐带病变所带来的诊断挑战,并强调了详细成像和手术探查对识别罕见先天性异常的重要性。组织病理学确认是准确诊断的必要条件。需要进一步的研究来阐明这些异常的胚胎学基础和临床意义。
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审稿时长
13 weeks
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