Murphy Jamie, Kalkbrenner Kristen A, Pemberton John H, Landmann Ron G, Heppell Jacques P, Young-Fadok Tonia M, Etzioni David A
1Division of Colon and Rectal Surgery, Mayo Clinic, Scottsdale, Arizona 2Division of Colon and Rectal Surgery, Mayo Clinic, Rochester, Minnesota 3Division of Colon and Rectal Surgery, Mayo Clinic, Jacksonville, Florida.
Dis Colon Rectum. 2014 Aug;57(8):993-8. doi: 10.1097/DCR.0000000000000172.
Endoscopic surveillance of patients with ulcerative colitis aims to prevent cancer-related morbidity through the detection and treatment of dysplasia. The literature to date varies widely with regard to the importance of dysplasia as a marker for colorectal cancer at the time of colectomy.
The aim of this study was to accurately characterize the extent to which the preoperative detection of dysplasia is associated with undetected cancer in patients with ulcerative colitis.
DESIGN/PATIENTS/SETTING: A retrospective chart review was conducted of patients undergoing surgery for colitis within the Mayo Clinic Health System between August 1993 and July 2012.
Patient demographics and pre- and postoperative dysplasia were tabulated. The relationship between pre- and postoperative dysplasia/cancer in surgical pathology specimens was assessed.
A total of 2130 patients underwent abdominal colectomy or proctocolectomy; 329 patients were identified (15%) as having at least 1 focus of dysplasia preoperatively. Of these 329 patients, the majority were male (69%) with a mean age of 49.7 years. Unsuspected cancer was found in 6 surgical specimens. Indeterminate dysplasia was not associated with cancer (0/50). Preoperative low-grade dysplasia was associated with a 2% (3/141) risk of undetected cancer when present in random surveillance biopsies and a 3% (2/79) risk if detected in endoscopically visible lesions. Similarly, 3% (1/33) of patients identified preoperatively with random surveillance biopsy high-grade dysplasia harbored undetected cancer. Unsuspected dysplasia was found in 62/1801 (3%) cases without preoperative dysplasia.
This study is limited by its retrospective nature and by its lack of evaluation of the natural history of dysplastic lesions that progress to cancer.
The presence of dysplasia was associated with a low risk of unsuspected cancer at the time of colectomy. These findings will help inform the decision-making process for patients with ulcerative colitis who are considering intensive surveillance vs surgical intervention after a diagnosis of dysplasia.
溃疡性结肠炎患者的内镜监测旨在通过检测和治疗发育异常来预防癌症相关的发病情况。迄今为止的文献在发育异常作为结肠切除术时结直肠癌标志物的重要性方面差异很大。
本研究的目的是准确描述溃疡性结肠炎患者术前检测到的发育异常与未检测到的癌症之间的关联程度。
设计/患者/地点:对1993年8月至2012年7月在梅奥诊所医疗系统内接受结肠炎手术的患者进行回顾性病历审查。
列出患者的人口统计学特征以及术前和术后的发育异常情况。评估手术病理标本中术前和术后发育异常/癌症之间的关系。
共有2130例患者接受了腹部结肠切除术或直肠结肠切除术;329例患者(15%)被确定术前至少有1个发育异常病灶。在这329例患者中,大多数为男性(69%),平均年龄49.7岁。6份手术标本中发现了意外癌症。不确定的发育异常与癌症无关(0/50)。术前低级别发育异常在随机监测活检中出现时,未检测到癌症的风险为2%(3/141),在内镜可见病变中检测到时,风险为3%(2/79)。同样,术前经随机监测活检确定为高级别发育异常的患者中有3%(1/33)存在未检测到的癌症。在1801例术前无发育异常的病例中有62例(3%)发现了意外的发育异常。
本研究受其回顾性性质的限制,且缺乏对进展为癌症的发育异常病变自然史的评估。
发育异常的存在与结肠切除术时意外癌症的低风险相关。这些发现将有助于为考虑在诊断发育异常后进行强化监测与手术干预的溃疡性结肠炎患者的决策过程提供信息。