Department of Internal Medicine, Texas Tech University Health Science Center El Paso, 2000B Transmountain Road, El Paso, TX 79911, USA; Paul L. Foster School of Medicine (PLFSOM), Texas Tech University Health Science Center El Paso, 5001 El Paso Dr, El Paso, TX 79905, USA.
Department of Internal Medicine, Texas Tech University Health Sciences Center, 4800 Alberta Avenue, El Paso, TX 79905, USA.
Dis Mon. 2019 Dec;65(12):100851. doi: 10.1016/j.disamonth.2019.02.004. Epub 2019 Mar 2.
Ulcerative colitis (UC) is a chronic idiopathic inflammatory bowel disorder of the colon that causes continuous mucosal inflammation extending from the rectum to the more proximal colon, with variable extents. UC is characterized by a relapsing and remitting course. UC was first described by Samuel Wilks in 1859 and it is more common than Crohn's disease worldwide. The overall incidence and prevalence of UC is reported to be 1.2-20.3 and 7.6-245 cases per 100,000 persons/year respectively. UC has a bimodal age distribution with an incidence peak in the 2nd or 3rd decades and followed by second peak between 50 and 80 years of age. The key risk factors for UC include genetics, environmental factors, autoimmunity and gut microbiota. The classic presentation of UC include bloody diarrhea with or without mucus, rectal urgency, tenesmus, and variable degrees of abdominal pain that is often relieved by defecation. UC is diagnosed based on the combination of clinical presentation, endoscopic findings, histology, and the absence of alternative diagnoses. In addition to confirming the diagnosis of UC, it is also important to define the extent and severity of inflammation, which aids in the selection of appropriate treatment and for predicting the patient's prognosis. Ileocolonoscopy with biopsy is the only way to make a definitive diagnosis of UC. A pathognomonic finding of UC is the presence of continuous colonic inflammation characterized by erythema, loss of normal vascular pattern, granularity, erosions, friability, bleeding, and ulcerations, with distinct demarcation between inflamed and non-inflamed bowel. Histopathology is the definitive tool in diagnosing UC, assessing the disease severity and identifying intraepithelial neoplasia (dysplasia) or cancer. The classical histological changes in UC include decreased crypt density, crypt architectural distortion, irregular mucosal surface and heavy diffuse transmucosal inflammation, in the absence of genuine granulomas. Abdominal computed tomographic (CT) scanning is the preferred initial radiographic imaging study in UC patients with acute abdominal symptoms. The hallmark CT finding of UC is mural thickening with a mean wall thickness of 8 mm, as opposed to a 2-3 mm mean wall thickness of the normal colon. The Mayo scoring system is a commonly used index to assess disease severity and monitor patients during therapy. The goals of treatment in UC are three fold-improve quality of life, achieve steroid free remission and minimize the risk of cancer. The choice of treatment depends on disease extent, severity and the course of the disease. For proctitis, topical 5-aminosalicylic acid (5-ASA) drugs are used as the first line agents. UC patients with more extensive or severe disease should be treated with a combination of oral and topical 5-ASA drugs +/- corticosteroids to induce remission. Patients with severe UC need to be hospitalized for treatment. The options in these patients include intravenous steroids and if refractory, calcineurin inhibitors (cyclosporine, tacrolimus) or tumor necrosis factor-α antibodies (infliximab) are utilized. Once remission is induced, patients are then continued on appropriate medications to maintain remission. Indications for emergency surgery include refractory toxic megacolon, colonic perforation, or severe colorectal bleeding.
溃疡性结肠炎(UC)是一种慢性特发性炎症性肠病,累及结肠,导致连续的黏膜炎症从直肠延伸至近端结肠,其程度不一。UC 的特征是反复发作和缓解。UC 是由 Samuel Wilks 于 1859 年首次描述的,它在全球范围内比克罗恩病更为常见。UC 的总体发病率和患病率分别为每 10 万人/年 1.2-20.3 例和 7.6-245 例。UC 的发病年龄呈双峰分布,发病高峰在 20 至 30 岁之间,其次是 50 至 80 岁之间。UC 的主要危险因素包括遗传、环境因素、自身免疫和肠道微生物群。UC 的典型表现包括血性腹泻伴或不伴黏液、直肠急迫感、里急后重,以及不同程度的腹痛,排便后常可缓解。UC 的诊断基于临床表现、内镜检查、组织学和排除其他诊断的综合结果。除了确诊 UC 外,还需要确定炎症的程度和严重程度,这有助于选择合适的治疗方法,并预测患者的预后。回肠结肠镜检查和活检是确诊 UC 的唯一方法。UC 的一个特征性发现是存在连续的结肠炎症,表现为红斑、正常血管模式丧失、颗粒状、糜烂、易碎、出血和溃疡,炎症和非炎症肠段之间有明显的分界。组织病理学是诊断 UC 的明确工具,可评估疾病严重程度和识别上皮内瘤变(异型增生)或癌症。UC 的经典组织学改变包括隐窝密度降低、隐窝结构变形、黏膜表面不规则和弥漫性黏膜下炎症,无真正的肉芽肿。腹部计算机断层扫描(CT)扫描是 UC 患者急性腹痛时首选的初始放射影像学研究。UC 的标志性 CT 发现是壁层增厚,平均壁厚度为 8mm,而正常结肠的平均壁厚度为 2-3mm。Mayo 评分系统是一种常用的评估疾病严重程度和监测治疗期间患者的指标。UC 治疗的目标是三重:提高生活质量、实现无激素缓解和最大限度降低癌症风险。治疗的选择取决于疾病的范围、严重程度和病程。对于直肠炎,局部应用 5-氨基水杨酸(5-ASA)药物是一线治疗药物。UC 患者有更广泛或严重的疾病,应采用口服和局部 5-ASA 药物联合/不联合皮质类固醇诱导缓解。需要住院治疗的 UC 患者包括静脉内应用皮质类固醇,如果治疗无效,可使用钙调神经磷酸酶抑制剂(环孢素、他克莫司)或肿瘤坏死因子-α 抗体(英夫利昔单抗)。一旦诱导缓解,患者就会继续使用适当的药物维持缓解。需要紧急手术的指征包括难治性中毒性巨结肠、结肠穿孔或严重结直肠出血。