Mazahreh Tagleb S, Aleshawi Abdelwahab J, Alorjani Mohammed S, Elayyan Rasheed, Al-Zoubi Nabil A
Department of General Surgery and Urology, Faculty of Medicine, Jordan University of Science & Technology, P. O. Box: 3030, Irbid, 22110, Jordan.
Department of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science & Technology, Irbid, 22110, Jordan.
BMC Surg. 2019 Jun 27;19(1):70. doi: 10.1186/s12893-019-0538-0.
Jejunal diverticula are the rarest of all small bowel diverticula. Most patients with jejunal diverticula are asymptomatic. Major complications include diverticulitis, gastrointestinal hemorrhage, intestinal obstruction and perforation. The hemorrhage has been attributed to diverticulitis with ulceration, diverticulosis associated with trauma and irritation disorder. However, only six cases reported the arteriovenous malformations within jejunal diverticulosis to be the cause of hemorrhage.
We present a case of arteriovenous malformations within jejunal diverticulosis in a 68-year-old male presented with lower gastrointestinal bleeding. After admission and stabilization, upper and lower endoscopies were performed without demonstrating the bleeding site. They only revealed clotted and red blood throughout the colon. Technetium-labeled red blood cell bleeding scan, endoscopic capsule, and selective angiography were performed to localize the site of bleeding without significant findings. As the clinical status of the patient deteriorated, exploratory laparotomy was performed urgently. Extensive jejunal saccular pouches were found 10 cm distal to duodenojejunal junction extending 1.6 m distally. Segmental resection was performed with side to side primary anastomosis. Microscopic examination of the specimen revealed many diverticula. He was followed up 2 years after that without complications.
We report yet the seventh case jejunal diverticulosis with the presence of angiodysplasia, in hope of expanding the knowledge of a rare occurrence and increasing the demand for further research about the etiology, clinical impact and treatment of such anomalies coexistence. This case also highlights the importance of considering the diagnosis of AVMs within jejunal diverticulosis in the presence of uncontrollable blood loss in the pre- or intra- operatively diagnosed jejunal diverticulosis and the urgent need for surgical intervention. In addition, the diagnostic tests should be performed close to the bleeding episode.
空肠憩室是所有小肠憩室中最罕见的。大多数空肠憩室患者无症状。主要并发症包括憩室炎、胃肠道出血、肠梗阻和穿孔。出血原因一直被认为是伴有溃疡的憩室炎、与创伤和刺激性疾病相关的憩室病。然而,仅有6例报道空肠憩室病内的动静脉畸形是出血原因。
我们报告一例68岁男性空肠憩室病合并动静脉畸形,表现为下消化道出血。入院病情稳定后,进行了上下消化道内镜检查,但未发现出血部位。内镜检查仅发现整个结肠内有凝血块和红色血液。进行了锝标记红细胞出血扫描、内镜胶囊检查和选择性血管造影以定位出血部位,但均无明显发现。随着患者临床状况恶化,紧急进行了剖腹探查术。在十二指肠空肠交界处远端10厘米处发现广泛的空肠囊状憩室,向远端延伸1.6米。进行了节段性切除并端端一期吻合。标本的显微镜检查显示有许多憩室。此后对其进行了2年随访,无并发症发生。
我们报告了第七例伴有血管发育异常的空肠憩室病病例,希望能扩展对这种罕见情况的认识,并增加对这种异常共存的病因、临床影响和治疗的进一步研究需求。该病例还强调了在术前或术中诊断为空肠憩室病且存在无法控制的失血时,考虑空肠憩室病内动静脉畸形诊断的重要性以及手术干预的迫切需要。此外,诊断检查应在出血发作时进行。