Wu Yang, Mullin Alexander, Stoita Alina
Department of Gastroenterology and Hepatology, St Vincent's Hospital, University of NSW, Sydney, NSW 2010, Australia.
University of Notre Dame, Sydney, NSW 2010, Australia.
World J Gastrointest Endosc. 2017 Sep 16;9(9):464-470. doi: 10.4253/wjge.v9.i9.464.
To compared individuals with serrated polyposis syndrome (SPS) to those with sessile serrated adenoma (SSA) and adenomas in the setting of endoscopists with high adenoma detection rates at a secondary and tertiary academic centre.
Retrospectively we collated the clinical, endoscopic and histological features of all patients with SPS at St Vincent's public and private hospital in the last 3 years. Patients were identified by searching through 2 pathology databases. Variables explored included smoking status, symptoms, and family history of concurrent colorectal cancer, number and location of polyps. Patients with SPS were matched to two cohorts (1) patients with SSA not meeting World Health Organization (WHO) criteria for SPS over 3 years; and (2) patients with exclusively adenomas. The control cases were also matched according to gender and endoscopist. Adenoma detection rates ranged from 25% to 40%.
Forty patients with SPS were identified and matched with 40 patients in each control group. In total 15452 colonoscopies were performed over the study period which amounts to a prevalence of 1: 384 patients (0.26%) with SPS. Fourteen patients (35%) required more than 1 year to accumulate enough polyps to reach WHO criteria for SPS. The diagnosis of SPS was largely incidental and 5% SPS patients were diagnosed with colorectal cancer over 3 years. The chance of detecting a meta-synchronous adenoma was similar in those with SPS (42%) and those with SSA (55%), = 0.49. The majority of patients (75%) meeting criteria for SPS were women. The mean age of those with SPS (45 years) was significantly lower than both cohorts with SSA (57 years) and adenomas (63 years), = 0.01. On univariate analysis cigarette exposure, first-degree family history of colorectal cancer and a high BMI weren't significantly more associated with SPS compared to patients with SSA or patients with adenomas. However, patients with SPS (97%) and patients with SSAs not meeting SPS criteria (98%) were significantly more likely to be Caucasian compared to patients with adenomas (79%), = 0.01.
The prevalence of SPS in our study was 0.26%. The vast majority of patients diagnosed with SPS were women. As a group, they were significantly younger compared to patients with SSA not meeting WHO criteria and patients with adenomatous polyps by more than a decade. Patients with SPS were no more likely to have a first degree relative with colorectal cancer or smoking history than the other two groups. Patients with serrated polyps were more likely to be Caucasian than patients with adenomas.
在一家二级和三级学术中心,将锯齿状息肉病综合征(SPS)患者与无蒂锯齿状腺瘤(SSA)患者及腺瘤患者进行比较,这些患者的内镜医师腺瘤检出率较高。
我们回顾性整理了过去3年在圣文森特公立医院和私立医院所有SPS患者的临床、内镜和组织学特征。通过搜索两个病理数据库来识别患者。探讨的变量包括吸烟状况、症状、同时患结直肠癌的家族史、息肉数量和位置。将SPS患者与两个队列进行匹配:(1)3年内不符合世界卫生组织(WHO)SPS标准的SSA患者;(2)仅患有腺瘤的患者。对照病例也根据性别和内镜医师进行匹配。腺瘤检出率在25%至40%之间。
确定了40例SPS患者,并与每个对照组的40例患者进行匹配。在研究期间共进行了15452例结肠镜检查,SPS的患病率为1:384例患者(0.26%)。14例患者(35%)需要超过1年的时间来积累足够的息肉以达到WHO的SPS标准。SPS的诊断大多是偶然的,5%的SPS患者在3年内被诊断为结直肠癌。SPS患者(42%)和SSA患者(55%)检测到异时性腺瘤的几率相似,P = 0.49。符合SPS标准的大多数患者(75%)为女性。SPS患者的平均年龄(45岁)显著低于SSA队列(57岁)和腺瘤队列(63岁),P = 0.01。单因素分析显示,与SSA患者或腺瘤患者相比,吸烟史、结直肠癌一级家族史和高体重指数与SPS的相关性并不显著。然而,与腺瘤患者(79%)相比,SPS患者(97%)和不符合SPS标准的SSA患者(98%)更可能是白种人,P = 0.01。
我们研究中SPS的患病率为0.26%。绝大多数被诊断为SPS的患者为女性。作为一个群体,他们比不符合WHO标准的SSA患者和腺瘤性息肉患者年轻十多年。与其他两组相比,SPS患者患结直肠癌的一级亲属或吸烟史的可能性并不更高。与腺瘤患者相比,锯齿状息肉患者更可能是白种人。