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5-氨基乙酰丙酸诱导原卟啉IX致敏后,对巴雷特食管、溃疡性结肠炎或腺瘤性息肉患者发育异常进行内镜荧光检测。

Endoscopic fluorescence detection of dysplasia in patients with Barrett's esophagus, ulcerative colitis, or adenomatous polyps after 5-aminolevulinic acid-induced protoporphyrin IX sensitization.

作者信息

Messmann H, Knüchel R, Bäumler W, Holstege A, Schölmerich J

机构信息

Departments of Internal Medicine I, Pathology and Dermatology, University of Regensburg, Germany.

出版信息

Gastrointest Endosc. 1999 Jan;49(1):97-101. doi: 10.1016/s0016-5107(99)70453-0.

Abstract

BACKGROUND

Surveillance of patients with Barrett's esophagus or ulcerative colitis for dysplasia is confined to biopsy specimens taken randomly during endoscopy because dysplasia remains undetectable by visual inspection. We attempted to visualize dysplastic tissue during endoscopy after sensitization with 5-aminolevulinic acid (5-ALA) leading to accumulation and formation of protoporphyrin IX and induction of characteristic red fluorescence of the latter substance using blue light illumination.

METHODS

Six patients with histologically proven low- or high-grade dysplasia (Barrett's esophagus 2, ulcerative colitis 1, Billroth-II stomach 1, rectal polyps 2) were treated with oral administration of different concentrations of 5-ALA (10 to 20 mg/kg) or by local instillation of 3 gm 5-ALA in the rectum. Endoscopic fluorescence detection was performed 1 to 6 hours after sensitization using a blue light source and compared with conventional white light endoscopy. Biopsies of fluorescent and nonfluorescent areas were compared with histologic findings.

RESULTS

Normal duodenal mucosa and squamous epithelium showed more intense 5-ALA-induced background red fluorescence compared with normal mucosa in the stomach or Barrett's mucosa. Histologically, dysplasia was exclusively found in areas with red fluorescence. False-positive fluorescence was associated with microscopic inflammation of the mucosa or feces in the colon.

CONCLUSIONS

5-ALA-induced protoporphyrin IX fluorescence may be useful in the detection of dysplasia in the gastrointestinal tract by enhancement of endoscopic surveillance of patients at a high risk for dysplasia.

摘要

背景

巴雷特食管或溃疡性结肠炎患者的发育异常监测仅限于在内镜检查期间随机采集的活检标本,因为通过肉眼检查无法检测到发育异常。我们尝试在用5-氨基乙酰丙酸(5-ALA)致敏后在内镜检查期间可视化发育异常组织,5-ALA可导致原卟啉IX积累并形成,使用蓝光照射可诱导后一种物质产生特征性红色荧光。

方法

对6例经组织学证实为低级别或高级别发育异常的患者(巴雷特食管2例、溃疡性结肠炎1例、毕罗-II式胃1例、直肠息肉2例),口服不同浓度的5-ALA(10至20mg/kg)或在直肠局部注入3g 5-ALA进行治疗。致敏后1至6小时,使用蓝光光源进行内镜荧光检测,并与传统白光内镜检查进行比较。对荧光和非荧光区域进行活检,并与组织学结果进行比较。

结果

与胃或巴雷特黏膜中的正常黏膜相比,正常十二指肠黏膜和鳞状上皮显示出更强的5-ALA诱导的背景红色荧光。组织学上,发育异常仅在有红色荧光的区域发现。假阳性荧光与黏膜的微观炎症或结肠中的粪便有关。

结论

5-ALA诱导的原卟啉IX荧光通过加强对发育异常高危患者的内镜监测,可能有助于检测胃肠道中的发育异常。

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