Gandhi Jignesh A, Shinde Pravin H, Churiwala Jayati J, Husain Sakina
Department of Surgery, Seth G.S. Medical College & K.E.M. Hospital, Mumbai, Maharashtra, India.
Surg J (N Y). 2021 Feb 1;7(1):e14-e17. doi: 10.1055/s-0040-1722180. eCollection 2021 Jan.
Enteric duplication cysts are a rare congenital abnormality that present more commonly in children than adults. Clinical presentation varies from vague abdominal pain, abdominal lump, iron deficiency anemia to intestinal obstruction due to intussusception or mass effect. We report a tubular ileal duplication in an adult male presenting with an acute abdomen due to perforative peritonitis. A 20-year-old male presented to the emergency department with complains of right lower abdominal pain. On clinical examination and ultrasound scan patient was suspected to have a complicated acute appendicitis (rupture). However, a computed tomography scan was suggestive of perforation in the distal ileum. Emergency exploratory laparotomy revealed a perforated isolated ileal tubular duplication.
肠重复囊肿是一种罕见的先天性异常,在儿童中比成人更常见。临床表现多样,从模糊的腹痛、腹部肿块、缺铁性贫血到因肠套叠或肿块效应导致的肠梗阻。我们报告一例成年男性因穿孔性腹膜炎出现急腹症,其存在管状回肠重复畸形。一名20岁男性因右下腹痛就诊于急诊科。经临床检查和超声扫描,怀疑患者患有复杂性急性阑尾炎(破裂)。然而,计算机断层扫描提示回肠远端穿孔。急诊剖腹探查发现一个孤立的穿孔性回肠管状重复畸形。