Al-Tarakji Mohannad, Almogtaba Mohamed, Al-Hashimy Yaseen, Moustafa Omar S, Shehata Mona S, Al-Zoubi Raed M, Ghali Mohamed Said
Department of Surgery, Acute Care Surgery Hamad Medical Corporation Doha Qatar.
Department of Surgery, General Surgery Hamad Medical Corporation Doha Qatar.
Clin Case Rep. 2024 Jan 17;12(1):e8395. doi: 10.1002/ccr3.8395. eCollection 2024 Jan.
In an 18-year-old, Meckel's diverticulum and a rare vitellointestinal fibrous band caused bowel obstruction. Clinicians should be vigilant for such anomalies, especially in young adults with virgin abdomens, as potential sources of intestinal obstruction.
In this case report, we highlight the rarity of vitellointestinal or omphalomesenteric duct anomalies causing intestinal obstruction in the adult population. The patient, an 18-year-old male, presented to the emergency department with a two-day history of abdominal pain and vomiting. Physical examination revealed mild distension of his virgin abdomen with generalized tenderness. Abdominal X-ray displayed dilated small bowel loops, and a computed tomography scan indicated features consistent with closed-loop bowel obstruction. Diagnostic laparoscopy confirmed a vitellointestinal duct remnant as the cause of the small intestinal obstruction, involving a combined Meckel's diverticulum and vitellointestinal fibrous band. In early fetal development, the vitellointestinal duct communicates between the midgut and the yolk sac, expected to disappear during fetal growth. Failure to obliterate can lead to issues such as intestinal blockage, primarily observed in children, making occurrences in adults, as in this case, infrequent with only a few documented instances. Despite its uncommon occurrence in young adults, healthcare providers should consider the vitellointestinal duct anomalous remnant as a potential source of intestinal obstruction, particularly in individuals with a virgin abdomen. Early detection of intestinal obstruction is imperative for patient survival, facilitating prompt management and minimizing the risk of serious morbidities, ultimately contributing to a better patient outcome.
一名18岁患者,梅克尔憩室和罕见的卵黄肠管纤维带导致肠梗阻。临床医生应警惕此类异常情况,尤其是在未生育过的年轻成年人中,将其视为肠梗阻的潜在病因。
在本病例报告中,我们强调卵黄肠管或脐肠系膜管异常在成年人群中导致肠梗阻的罕见性。该患者为一名18岁男性,因腹痛和呕吐两天就诊于急诊科。体格检查发现其未生育过的腹部轻度膨胀,有广泛压痛。腹部X线显示小肠肠袢扩张,计算机断层扫描显示符合闭袢性肠梗阻的特征。诊断性腹腔镜检查证实卵黄肠管残余物是小肠梗阻的病因,涉及合并的梅克尔憩室和卵黄肠管纤维带。在胎儿早期发育过程中,卵黄肠管在中肠和卵黄囊之间相通,预计在胎儿生长过程中消失。未能闭塞可导致诸如肠梗阻等问题,主要见于儿童,像本病例这样发生在成年人中的情况很少见,仅有少数文献记载的病例。尽管在年轻成年人中发生率不高,但医疗服务提供者应将卵黄肠管异常残余物视为肠梗阻的潜在病因,尤其是在未生育过的个体中。早期发现肠梗阻对患者生存至关重要,有助于及时处理并将严重并发症的风险降至最低,最终改善患者预后。