Mohiuddin S Sameer, Gonzalez Adolfo, Corpron Cynthia
JSLS. 2011 Oct-Dec;15(4):558-61. doi: 10.4293/108680811X13176785204553.
Meckel's diverticulum is a congenital anomaly resulting from incomplete obliteration of the omphalomesenteric duct. The incidence ranges from 0.3% to 2.5% with most patients being asymptomatic. In some cases, complications involving a Meckel's diverticulum may mimic other disease processes and obscure the clinical picture.
This case presents an 8-year-old male with abdominal pain, nausea, and vomiting and an examination resembling appendicitis.
A CT scan revealed findings consistent with appendicitis with dilated loops of small bowel. During laparoscopic appendectomy, the appendix appeared unimpressive, and an inflamed Meckel's diverticulum was found with an adhesive band creating an internal hernia with small bowel obstruction. The diverticulum was resected after the appendix was removed.
The incidence of an internal hernia with a Meckel's diverticulum is rare. A diseased Meckel's diverticulum can be overlooked in many cases, especially in those resembling appendicitis. It is recommended that the small bowel be assessed in all appendectomy cases for a pathological Meckel's diverticulum.
梅克尔憩室是一种先天性异常,由卵黄管未完全闭塞所致。发病率为0.3%至2.5%,大多数患者无症状。在某些情况下,涉及梅克尔憩室的并发症可能会模仿其他疾病过程并掩盖临床表现。
本病例为一名8岁男性,有腹痛、恶心和呕吐症状,检查结果类似阑尾炎。
CT扫描显示结果与阑尾炎相符,小肠肠袢扩张。在腹腔镜阑尾切除术中,阑尾外观无异常,发现一个发炎的梅克尔憩室,有一条粘连带形成内疝并导致小肠梗阻。阑尾切除后,憩室被切除。
梅克尔憩室内疝的发病率罕见。在许多情况下,患病的梅克尔憩室可能被忽视,尤其是在那些类似阑尾炎的病例中。建议在所有阑尾切除病例中评估小肠是否存在病理性梅克尔憩室。