Stancu Samantha Mc Kenzie, Popescu Bogdan Aurelian, Beuran Mircea
Chirurgia (Bucur). 2016 May-Jun;111(3):270-3.
Meckel's Diverticulum is the most common congenital malformation of the gastrointestinal tract with a prevalence of 2 % in the general population, being twice as common and symptomatic in males. Not seldom is the diagnosis made incidentally, upon laparotomy for other intra-abdominal conditions, namely acute appendicitis. Simple Diverticulectomy is the surgical treatment of choice. We present the case of S.M., a 38 year-old male who was admitted to the Surgery Department of the Bucharest Clinical Emergency Hospital for sudden onset of initially periumbilical pain, which later migrated and localized in the right iliac fossa (RIF) accompanied by vomiting after the onset of pain, approximately 24 hours prior to admission. Examination of the abdomen revealed localized peritoneal signs. An Alvarado score of 8 was calculated. A laparotomy for appendectomy was performed, upon which the sigmoid colon was found in the RIF, and an appendix of 10 cm in length was visualized in a subhepatic, ascendant position. At a distance of 90 cm from the ileocecal valve, a Meckel's Diverticulum with dimensions of 7/4 cm was discovered. A retrograde appendectomy was performed first, along with a simple diverticulectomy, with the use of a TA 30 mm stapler. The operative time was 90 minutes without intraoperative complications, and an uneventful postoperative recovery, culminating with discharge of the patient on the fifth postoperative day. Despite its high prevalence, Meckel's Diverticulum still represents a diagnostic challenge, especially in the adult population, notably in asymptomatic patients. Moreover, ectopic gastric or pancreatic tissue, present in 50% of the cases, leads to a vast array of differential diagnoses. Due to its numerous life-threatening complications such as bleeding, intestinal obstruction, volvulus, intussusception, diverticulitis, fistulization and perforation, accurate diagnosis and timely treatment is crucial.
梅克尔憩室是最常见的胃肠道先天性畸形,在普通人群中的患病率为2%,男性的发病率和症状出现频率是女性的两倍。该疾病常因其他腹腔内疾病(如急性阑尾炎)行剖腹手术时偶然被诊断出来。单纯憩室切除术是首选的手术治疗方法。我们报告了S.M.的病例,这是一名38岁男性,因突发最初位于脐周的疼痛而入住布加勒斯特临床急诊医院外科,疼痛随后转移并定位在右下腹,疼痛发作后约24小时入院,伴有呕吐。腹部检查发现局部腹膜征。计算得出阿尔瓦拉多评分为8分。进行了阑尾切除术的剖腹手术,术中发现乙状结肠位于右下腹,在肝下上升位置可见一个10厘米长的阑尾。在距回盲瓣90厘米处,发现一个大小为7/4厘米的梅克尔憩室。首先进行了逆行阑尾切除术,同时使用TA 30毫米吻合器进行了单纯憩室切除术。手术时间为90分钟,无术中并发症,术后恢复顺利,患者于术后第五天出院。尽管梅克尔憩室患病率很高,但它仍然是一个诊断难题,尤其是在成年人群中,特别是无症状患者。此外,50%的病例中存在异位胃或胰腺组织,这导致了大量的鉴别诊断。由于其众多危及生命的并发症,如出血、肠梗阻、肠扭转、肠套叠、憩室炎、瘘管形成和穿孔,准确诊断和及时治疗至关重要。