Management of colorectal polyps

IF 232.4 1区 医学 Q1 ONCOLOGY CA: A Cancer Journal for Clinicians Pub Date : 1997-03-01 DOI:10.3322/canjclin.47.2.93
Dr. Arnold J. Markowitz MD, Dr. Sidney J. Winawer MD
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引用次数: 66

Abstract

A colorectal polyp is defined as a visible protrusion above the surface of the surrounding normal large bowel mucosa. Polyps may be detected endoscopically by sigmoidoscopy or colonoscopy, or radiographically by barium enema.

Colorectal polyps are classified histologically as either neoplastic (adenomatous polyps) or non-neoplastic (Table). Although all adenomatous polyps have malignant potential, the majority are benign when detected. In contrast, hyper-plastic, mucosal, inflammatory, and hamartomatous polyps are non-neoplastic and thus have no malignant potential. Lastly, submucosal polyps include lymphoid polyps, lipomas, and other less common histologic types.

Appropriate management of colorectal polyps requires an understanding of the typical clinical presentation, anatomic distribution, and associated clinical findings of these variable histologic types. Furthermore, although most colorectal polyps occur sporadically, some may be associated with a hereditary syndrome, such as familial adenomatous polyposis (FAP), juvenile polyposis, Peutz-Jeghers, or hereditary nonpolyposis colorectal cancer (HNPCC).

Adenomatous and hyperplastic polyps are the most commonly detected colorectal polyps and are the most likely to be found during screening sigmoidoscopy. In this article we review the epidemiology, diagnosis, initial management, and follow-up surveillance of each polyp type. We discuss the indications for biopsy and removal of polyps found at sigmodoscopy and colonoscopy and the need for further evaluation and follow-up. Additionally, we cover the diagnostic criteria, clinical manifestations, malignant potential, and recommendations for polyp management and surveillance in the associated hereditary syndromes.

Submucosal colorectal lesions may protrude into the bowel lumen and produce a polypoid appearance. Colonoscopic biopsies of these lesions are usually non-diagnostic because the biopsies are too superficial and sample only the normal overlying mucosa. Multiple sequential biopsies at a single location may obtain a piece of the underlying submucosal tissue and provide a definitive diagnosis.

A national multi-institutional screening colonoscopy trial is currently being organized to investigate whether a single lifetime screening colonoscopy will decrease the incidence and mortality of colorectal cancer in the general population.

A new and innovative radiographic examination of the colon and rectum (computed tomographic colography or “virtual colonoscopy”) is currently being developed.98 This technique is noninvasive; if it is found to be sensitive and cost-effective, it may be used in the future for general population screening for colorectal polyps and cancers.

Noninvasive stool screening for specific genetic alterations, such as ras mutations,99 and biochemical abnormalities, such as elevations in decay-accelerating factor,100 may offer another potential approach for the detection of colorectal adenomas and cancers in the general population.

Genetic testing studies in families with HNPCC will help in the development of optimal screening and surveillance strategies for these individuals.

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结肠息肉的处理
结直肠息肉是指正常大肠黏膜表面上可见的突出物。息肉可在内镜下通过乙状结肠镜或结肠镜检查,或钡剂灌肠造影检查。结直肠息肉在组织学上分为肿瘤性(腺瘤性息肉)和非肿瘤性(表)。虽然所有的腺瘤性息肉都有恶性的可能,但大多数发现时是良性的。相反,过度增生、粘膜性、炎症性和错构瘤性息肉是非肿瘤性的,因此没有恶性潜能。最后,粘膜下息肉包括淋巴样息肉、脂肪瘤和其他不常见的组织学类型。结肠息肉的适当治疗需要了解这些不同组织学类型的典型临床表现、解剖分布和相关临床表现。此外,虽然大多数结直肠息肉是偶发的,但有些可能与遗传综合征有关,如家族性腺瘤性息肉病(FAP)、少年性息肉病、Peutz-Jeghers或遗传性非息肉性结直肠癌(HNPCC)。腺瘤性和增生性息肉是最常被发现的结直肠息肉,也是最容易在乙状结肠镜检查中被发现的。在本文中,我们回顾流行病学,诊断,初始管理和随访监测的每一种类型的息肉。我们讨论在乙状结肠镜检查和结肠镜检查中发现的息肉活检和切除的适应症,以及进一步评估和随访的必要性。此外,我们涵盖诊断标准,临床表现,恶性潜能,并建议息肉管理和监测相关的遗传综合征。结直肠粘膜下病变可突入肠腔,形成息肉样外观。这些病变的结肠镜活检通常是非诊断性的,因为活检太肤浅,只取样正常的覆盖粘膜。在单一位置进行多次连续活检可获得下层粘膜组织的一片,并提供明确的诊断。目前正在组织一项全国多机构筛查结肠镜试验,以调查单次终身筛查结肠镜检查是否会降低一般人群中结直肠癌的发病率和死亡率。98 .目前正在发展一种新的和创新的结肠和直肠放射检查(计算机断层摄影或“虚拟结肠镜检查”)这项技术是非侵入性的;如果发现它是敏感的和经济的,它可能在未来用于一般人群筛查结肠直肠息肉和癌症。无创粪便筛查特异性基因改变,如ras突变99和生化异常,如衰变加速因子升高100,可能为检测普通人群中的结直肠腺瘤和癌症提供另一种潜在方法。在HNPCC家庭中进行基因检测研究将有助于为这些个体制定最佳筛查和监测策略。
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来源期刊
CiteScore
873.20
自引率
0.10%
发文量
51
审稿时长
1 months
期刊介绍: CA: A Cancer Journal for Clinicians" has been published by the American Cancer Society since 1950, making it one of the oldest peer-reviewed journals in oncology. It maintains the highest impact factor among all ISI-ranked journals. The journal effectively reaches a broad and diverse audience of health professionals, offering a unique platform to disseminate information on cancer prevention, early detection, various treatment modalities, palliative care, advocacy matters, quality-of-life topics, and more. As the premier journal of the American Cancer Society, it publishes mission-driven content that significantly influences patient care.
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