O'Leary Michael P, Ashman Zane W, Plurad David S, Kim Dennis Y
Department of Surgery, Harbor-UCLA Medical Center, Torrance, CA, USA.
Case Rep Surg. 2016;2016:3247087. doi: 10.1155/2016/3247087. Epub 2016 Nov 9.
. A patent urachus is a rare congenital or acquired pathology, which can lead to complications later in life. We describe a case of urachal cystitis as the etiology of small bowel obstruction in an adult without prior intra-abdominal surgery. . A 64-year-old male presented to the acute care surgery team with a 5-day history of right lower quadrant abdominal pain, distention, nausea, and vomiting. He had a two-month history of urinary retention and his past medical history was significant for benign prostate hyperplasia. On exam, he had evidence of small bowel obstruction. Computed tomography revealed high-grade small bowel obstruction secondary to presumed ruptured appendicitis. In the operating room, an infected urachal cyst was identified with adhesions to the proximal ileum. After lysis of adhesions and resection of the cyst, the patient was subsequently discharged without further issues. . Although rare, urachal pathology should be considered in the differential diagnosis when evaluating a patient with small bowel obstruction without prior intraabdominal surgery, hernia, or malignancy.
脐尿管未闭是一种罕见的先天性或后天性病变,可在日后生活中导致并发症。我们描述了一例脐尿管膀胱炎作为一名无既往腹腔内手术史的成年人小肠梗阻病因的病例。一名64岁男性因右下象限腹痛、腹胀、恶心和呕吐5天就诊于急性护理外科团队。他有两个月的尿潴留病史,既往病史中良性前列腺增生较为显著。体格检查时,有小肠梗阻的证据。计算机断层扫描显示继发于推测的阑尾炎破裂的高位小肠梗阻。在手术室中,发现一个感染的脐尿管囊肿与近端回肠粘连。在粘连松解和囊肿切除术后,患者随后顺利出院,无进一步问题。尽管罕见,但在评估无既往腹腔内手术、疝气或恶性肿瘤的小肠梗阻患者时,鉴别诊断中应考虑脐尿管病变。