Jiang Guangyi, Fu Baojuan, Lv Sheng, Hong Junjie, Cai Xiujun
Department of General Surgery Key Laboratory of Laparoscopic Technology of Zhejiang Province, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou Department of General Surgery, Guang Fu Hospital, Jinhua, Zhejiang, China.
Medicine (Baltimore). 2017 Apr;96(15):e6589. doi: 10.1097/MD.0000000000006589.
Situs inversus totalis (SIT) is an uncommon clinical manifestation. Patients with SIT typically have malformation in the thorax and abdomen. The incidence of SIT ranges from 1/10,000 to 1/20,000 (Al-Jumaily and Hoche. J Laparoendosc Adv Surg Tech A 2001;11:229). Jejunojejunal intussusception is a rare complication after Roux-en-Y gastric bypass. Intussusception in adult cases accounts for 5% of adult intestinal obstruction cases, while in children, the occurrence is high and the majority of them are idiopathic cases.
Here, we present an uncommon case of jejunojejunal intussusception after Roux-en-Y gastric bypass in an SIT patient. We performed reduction at the beginning and resection was done finally.
We explore the potential causes and discuss the diagnosis and therapy.
Intussusception in an SIT patient is an uncommon case. The symptoms are vague, and it is difficult to diagnose. Clinicians should be vigilant postoperatively, especially when abdominal pain after gastrointestinal surgery occurs. It is a rare case worth learning.
全内脏反位(SIT)是一种罕见的临床表现。SIT患者通常在胸部和腹部存在畸形。SIT的发病率在1/10,000至1/20,000之间(Al-Jumaily和Hoche。《腹腔镜与内镜外科进展技术A》2001年;11:229)。空肠空肠套叠是Roux-en-Y胃旁路术后一种罕见的并发症。成人肠套叠病例占成人肠梗阻病例的5%,而在儿童中,发病率较高,且大多数为特发性病例。
在此,我们呈现一例SIT患者在Roux-en-Y胃旁路术后发生空肠空肠套叠的罕见病例。我们最初进行了复位,最终进行了切除。
我们探讨了潜在病因,并讨论了诊断和治疗方法。
SIT患者发生肠套叠是一种罕见病例。症状不明确,难以诊断。临床医生术后应保持警惕,尤其是在胃肠手术后出现腹痛时。这是一个值得学习的罕见病例。