Jarvis Johnathan K, Rambhajan Amrit
General Surgery, General Hospital Port of Spain, Port of Spain, TTO.
Cureus. 2020 Dec 26;12(12):e12305. doi: 10.7759/cureus.12305.
Intestinal malrotation (IM) is a congenital aberrancy of midgut rotation during development, which manifests among neonates more than adults. Older reports have estimated an incidence of one in 6,000 live births, which is now as high as one in 500. This congenital anomaly is generally indolent in the adult population. Recent literature research has failed to reveal any publications regarding the incidence within a Caribbean population. This paper aims to discuss the isolated case of a patient with this rare condition, who presented to a non-paediatric centre in Trinidad. This case highlights the implications of the initial radiological interpretation in conjunction with perioperative and intraoperative decision making. An 18-year-old male presented with a one-day history of abdominal pain, radiating to the epigastrium with nausea and excessive vomiting. Vital signs and blood investigations were normal. Initial CT scan results were interpreted as an internal hernia, which was surgically managed as such. Repeat imaging and a second laparotomy were required to correctly diagnose and perform the appropriate Ladd procedure. IM occurs due to the arrest of rotation of the midgut during fetal maturation. The incomplete rotation variant was seen in this case and is predominantly responsible for the symptomatology and morbidity associated with adult intestinal malrotation (AIM). Stringer has classified these anomalies based on the stage of embryonic development that is disrupted. CT helps with diagnostics in 97.5% of cases. This case highlights the implication of incorrect assessment on imaging and how it may misguide the interpretation of the findings at laparotomy leading to inappropriate surgical procedures. As many as 20% of cases undergo surgery without adult intussusception diagnosed. The incidence of IM seems to have increased but is scarcely encountered in the adult setting. When encountering this condition at a low-volume centre in the Caribbean, the adult specialist may be blindsided, and unknowingly underprepared without a high index of suspicion. Diagnosis at childhood should be discussed with the family and again with the patient on approaching adulthood. Patient education may help with the surgical assessment.
肠旋转不良(IM)是一种发育过程中中肠旋转的先天性异常,在新生儿中的表现比成人更为常见。较早的报告估计其在活产婴儿中的发病率为1/6000,现在高达1/500。这种先天性异常在成年人群中通常较为隐匿。最近的文献研究未能发现任何关于加勒比人群发病率的出版物。本文旨在讨论一名患有这种罕见疾病的患者的孤立病例,该患者就诊于特立尼达的一家非儿科中心。该病例突出了初始放射学解释与围手术期和术中决策的关联。一名18岁男性,有一天的腹痛病史,疼痛放射至上腹部,伴有恶心和频繁呕吐。生命体征和血液检查正常。最初的CT扫描结果被解读为内疝,并据此进行了手术处理。需要重复成像和再次剖腹手术才能正确诊断并进行适当的Ladd手术。IM是由于胎儿成熟过程中中肠旋转停止所致。本病例中可见不完全旋转变异型,这主要是导致成人肠旋转不良(AIM)相关症状和发病的原因。Stringer根据胚胎发育受阻的阶段对这些异常进行了分类。CT在97.5%的病例中有助于诊断。该病例突出了成像评估错误的影响,以及它如何可能误导剖腹手术中对发现的解读,导致不适当的手术操作。多达20%的病例在未诊断出成人肠套叠的情况下接受了手术。IM的发病率似乎有所增加,但在成人病例中很少见。在加勒比地区的低容量中心遇到这种情况时,成人专科医生可能会措手不及,在没有高度怀疑指数的情况下不知不觉地准备不足。儿童期的诊断应与家属讨论,并在患者接近成年时再次与患者讨论。患者教育可能有助于手术评估。