Strong procedure with added anchoring stitches from the jejunum to the abdominal wall for Superior Mesenteric Artery Syndrome in children: A case report

IF 0.2 Q4 PEDIATRICS Journal of Pediatric Surgery Case Reports Pub Date : 2025-05-01 Epub Date: 2025-02-24 DOI:10.1016/j.epsc.2025.102977
Abdulaziz Abdulrahman AlQahtani, Rula Sallout, Walid Tareef, Majid Alkhamis
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Abstract

Introduction

Sanjad-Sakati Syndrome (SSS) is a rare autosomal recessive disorder primarily observed in the Middle East. Superior mesenteric artery syndrome (SMAS) is also a rare gastrointestinal condition that mainly occurs in individuals who experience rapid weight loss and/or have a very low body mass index (BMI). The occurrence of these conditions together is extremely rare.

Case presentation

An 8-year-old girl with SSS was admitted to the hospital with flu-like symptoms, shortness of breath, and reduced oral intake over the previous two days. Her medical history included a recent right lobar pneumonia and recurrent vomiting. She was admitted with a diagnosis of recurrent pneumonia and received intravenous antibiotics. We placed a nasogastric tube, which drained bilious fluid. She underwent a plain abdominal film, an upper gastrointestinal study, and a computerized tomography (CT) scan which revealed that she had SMAS. She was started on conservative management, which included parenteral nutrition, metoclopramide, and small volume of enteral feedings. After four weeks without any improvement, we decided to proceed with a modified Strong operation. The modification involved anchoring the first segment of the jejunum to the abdominal wall of the right upper quadrant using two stitches of absorbable material, with the goal of minimizing the chance of a recurrence by preventing the jejunum from slipping back to its normal anatomical position. She tolerated the operation well. After an uneventful recovery, oral feedings were gradually introduced and increased until she reached full volume by postoperative day 12, She was discharged home one day later. She was followed for nine months and to date she has shown adequate weight gain.

Conclusion

Even though the association is remarkably rare, patients with SSS who had failure to thrive should undergo testing to rule out SMAS. If SMAS is confirmed and conservative measures are not successful, the modified Strong procedure appears to be a safe and effective surgical option.
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从空肠到腹壁添加锚定针的强力手术治疗儿童肠系膜上动脉综合征1例报告
sanjad - sakati综合征(SSS)是一种罕见的常染色体隐性遗传病,主要见于中东地区。肠系膜上动脉综合征(SMAS)也是一种罕见的胃肠道疾病,主要发生在体重迅速下降和/或体重指数(BMI)非常低的个体。这些情况同时发生是极其罕见的。病例介绍:一名8岁SSS女童在过去两天因流感样症状、呼吸急促和口服摄入量减少而入院。她的病史包括近期右大叶性肺炎和反复呕吐。她被诊断为复发性肺炎并接受静脉注射抗生素。我们放置了一根鼻胃管,引流胆汁。她接受了腹部平片、上胃肠道检查和计算机断层扫描(CT),结果显示她患有SMAS。她开始接受保守治疗,包括肠外营养、甲氧氯普胺和小容量肠内喂养。四周没有任何好转,我们决定进行一个改良的Strong手术。改良包括使用两针可吸收材料将空肠的第一段固定在右上象限的腹壁上,目的是通过防止空肠滑回其正常解剖位置来减少复发的机会。她能很好地忍受手术。在平稳恢复后,逐渐引入并增加口服喂养,直到术后第12天达到全容量,1天后出院回家。她被跟踪了9个月,到目前为止,她已经显示出足够的体重增加。结论:尽管这种关联非常罕见,但发育失败的SSS患者应该接受检测以排除SMAS。如果确认SMAS,保守措施不成功,改良的Strong手术似乎是一种安全有效的手术选择。
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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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