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首次在家族性腺瘤性息肉病患者及接受结肠切除术患者的回肠黏膜中观察到微腺瘤。

First observation of microadenomas in the ileal mucosa of patients with familial adenomatous polyposis and colectomies.

作者信息

Bertoni G, Sassatelli R, Nigrisoli E, Tansini P, Roncucci L, Ponz de Leon M, Bedogni G

机构信息

Department of Digestive Endoscopy, Ospedale S. Maria Nuova, Reggio Emilia, Italy.

出版信息

Gastroenterology. 1995 Aug;109(2):374-80. doi: 10.1016/0016-5085(95)90323-2.

Abstract

BACKGROUND & AIMS: Little data are available on the type and prevalence of mucosal changes involved in the development of ileal adenomas in patients with familial adenomatous polyposis who have undergone colectomy. However, colonic metaplasia of the ileal epithelium is thought to be an important step in the development of such adenomas.

METHODS

Retrograde endoscopy and biopsy of the distal ileum were performed in 17 affected patients who underwent total colectomy or proctocolectomy 3-184.1 months (mean, 80.3 +/- 13.9 months) before the study.

RESULTS

Macroscopic ileal polyps were identified in 14 (82.4%) patients. All polyps were sessile and 1-5 mm in size. Histological analysis showed adenomas in 9 (52.9%) patients and lymphoid hyperplasia or inflammation in the others. In 1 patient, an area of colonic-type metaplasia of the ileal mucosa was found close to an adenoma. However, in 5 (29.4%) patients, random biopsy specimens of the normal-appearing mucosa showed foci of abnormal crypts in the absence of metaplasia, with histological appearance similar to the findings described in dysplastic aberrant crypt foci of the colon. Such lesions, previously observed only in colorectal mucosa and referred to as microadenomas or oligocryptal adenomas, are considered putative preneoplastic abnormalities.

CONCLUSIONS

Although the hypothesized sequence normal ileal mucosa leading to colonic-type metaplasia leading to adenoma cannot be excluded, our findings support the sequence normal ileal mucosa leading to microadenoma leading to gross adenoma and possibly cancer as the main histogenetic pathway, as already suggested for the large bowel.

摘要

背景与目的

对于接受结肠切除术的家族性腺瘤性息肉病患者,有关回肠腺瘤发生过程中黏膜变化的类型和发生率的数据较少。然而,回肠上皮的结肠化生被认为是此类腺瘤发生的重要步骤。

方法

对17例受影响患者进行了回肠末端逆行内镜检查和活检,这些患者在研究前3 - 184.1个月(平均80.3±13.9个月)接受了全结肠切除术或直肠结肠切除术。

结果

14例(82.4%)患者发现了肉眼可见的回肠息肉。所有息肉均为无蒂,大小为1 - 5毫米。组织学分析显示,9例(52.9%)患者为腺瘤,其他患者为淋巴组织增生或炎症。在1例患者中,在靠近腺瘤处发现了回肠黏膜的结肠型化生区域。然而,在5例(29.4%)患者中,外观正常黏膜的随机活检标本显示在无化生的情况下存在异常隐窝灶,其组织学表现与结肠发育异常的异常隐窝灶中所描述的发现相似。此类病变以前仅在结直肠黏膜中观察到,被称为微腺瘤或少隐窝腺瘤,被认为是假定的肿瘤前异常。

结论

虽然不能排除正常回肠黏膜导致结肠型化生进而导致腺瘤的假设序列,但我们的研究结果支持正常回肠黏膜导致微腺瘤进而导致肉眼可见腺瘤并可能发展为癌症的序列作为主要的组织发生途径,正如之前对大肠所建议的那样。

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