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巴雷特食管的发育异常。6例患者的临床病理研究。

Dysplasia in Barrett's esophagus. A clinicopathologic study of six patients.

作者信息

Lee R G

出版信息

Am J Surg Pathol. 1985 Dec;9(12):845-52. doi: 10.1097/00000478-198512000-00001.

Abstract

To evaluate the consequences of dysplasia in Barrett's esophagus, six patients with esophageal mucosal biopsies showing dysplastic Barrett's mucosa in the absence of clinically evident esophageal carcinoma were identified and their clinicopathologic features reviewed. The patients, four men and two women, averaged 60 years and had long histories of gastroesophageal reflux. Four patients had high-grade dysplasia; two had low-grade. Dysplastic Barrett's mucosa appeared to arise most commonly from specialized-type Barrett's mucosa. After a mean follow-up of 29 months, four patients, all with high-grade dysplasia, had esophageal resections. Three of the four were found to have invasive adenocarcinoma, which extended through the esophageal wall in two patients. The fourth patient had a noninvasive adenomatous polyp ("Barrett's adenoma"), an infrequently described form of dysplasia in Barrett's esophagus. The two patients with low-grade dysplasia had developed no clinical indications of carcinoma. The results confirm that dysplastic Barrett's mucosa, particularly the high grade, is a morphologic marker for adenocarcinoma. Biopsy surveillance of patients with Barrett's esophagus is histologically feasible, but prospective studies are required to prove its effectiveness.

摘要

为评估巴雷特食管发育异常的后果,我们确定了6例食管黏膜活检显示为发育异常的巴雷特黏膜但无临床明显食管癌的患者,并回顾了他们的临床病理特征。这些患者中,4名男性,2名女性,平均年龄60岁,有长期胃食管反流病史。4例为高级别发育异常;2例为低级别。发育异常的巴雷特黏膜似乎最常起源于特殊类型的巴雷特黏膜。平均随访29个月后,4例均为高级别发育异常的患者接受了食管切除术。4例中的3例被发现患有浸润性腺癌,其中2例癌组织侵及食管壁。第4例患者有一个非浸润性腺瘤性息肉(“巴雷特腺瘤”),这是巴雷特食管中一种较少描述的发育异常形式。2例低级别发育异常的患者未出现癌症的临床指征。结果证实,发育异常的巴雷特黏膜,尤其是高级别者,是腺癌的形态学标志物。对巴雷特食管患者进行活检监测在组织学上是可行的,但需要前瞻性研究来证明其有效性。

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