Alzahrani Lujain, Joueidi Faisal, Abodahab Fawzy Mohamed, Joueidi Khaled, Khan Asim
Department of Pediatric Surgery, Maternity and Children Hospital, Makkah, Saudi Arabia.
College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Int J Surg Case Rep. 2024 Apr;117:109495. doi: 10.1016/j.ijscr.2024.109495. Epub 2024 Mar 11.
Cecal volvulus is a rare intestinal pathology that occurs due to abnormal cecum mobility associated with spectrum of complications. It is usually manifested in adults. However, on extremely rare occasions, it occurs in pediatrics. We presented a case of cecal volvulus demonstrating the significance of early diagnosis and treatment to reach successful outcomes.
A 12 year old boy who presented to the emergency department for clinical evaluation for acute abdomen. History and clinical examination was suggestive of acute bowel obstruction. Abdominal x-ray showed a large, distended gas filled viscus with base pointed towards the right lower quadrant. On the bases of radiological investigations, diagnosis of cecal volvolus made. Accordingly, the patient underwent emergency exploratory laparotomy. The post operative course was uneventful and was discharged in stable condition.
Cecal volvulus is an extremely rare manifestation of intestinal obstruction and malrotation. The clinical presentation of cecal volvulus depending on the duration and extent of the involvement of cecal malrotation The exact pathogenesis of cecal volvulus is unclear. However the association of the embryological development of the colon, affects the attachment to the posterior parietal peritoneum after ordinary anatomical rotation of 270°. The core-stone management of cecal volvulus is surgical approach.
Cecal volvulus requires a high index of suspicion and delicate care by the pediatric surgeon as it is considered an extremely rare entity in this age group. We highlighted the significance of early diagnosis, surgical treatment and the possibility of developing postoperative complications if left untreated.
盲肠扭转是一种罕见的肠道病变,由于盲肠活动异常并伴有一系列并发症而发生。它通常在成人中出现。然而,在极少数情况下,也会发生于儿科患者。我们报告了一例盲肠扭转病例,展示了早期诊断和治疗以取得成功结果的重要性。
一名12岁男孩因急性腹痛到急诊科进行临床评估。病史和临床检查提示急性肠梗阻。腹部X线显示一个巨大的、充满气体的扩张脏器,其底部指向右下腹。基于影像学检查,诊断为盲肠扭转。因此,患者接受了急诊剖腹探查术。术后过程顺利,出院时情况稳定。
盲肠扭转是肠梗阻和肠旋转不良的一种极其罕见的表现。盲肠扭转的临床表现取决于盲肠旋转不良的持续时间和累及范围。盲肠扭转的确切发病机制尚不清楚。然而,结肠的胚胎发育关联,在正常270°解剖旋转后影响其与后腹膜壁层的附着。盲肠扭转的核心治疗方法是手术。
盲肠扭转需要儿科外科医生高度怀疑并精心护理,因为在这个年龄组中它被认为是极其罕见的疾病。我们强调了早期诊断、手术治疗的重要性,以及如果不治疗可能出现术后并发症的情况。