Endoscopic fluorescence detection of dysplasia in patients with Barrett's esophagus, ulcerative colitis, or adenomatous polyps after 5-aminolevulinicacid-induced protoporphyrin IX sensitization
H. Messmann et al., Endoscopic fluorescence detection of dysplasia in patients with Barrett's esophagus, ulcerative colitis, or adenomatous polyps after 5-aminolevulinicacid-induced protoporphyrin IX sensitization, GASTROIN EN, 49(1), 1999, pp. 97-101
Background: Surveillance of patients with Barrett's esophagus or ulcerative
colitis for dysplasia is confined to biopsy specimens taken randomly durin
g endoscopy because dysplasia remains undetectable by visual inspection. We
attempted to visualize dysplastic tissue during endoscopy after sensitizat
ion with 5-aminolevulinic acid (5-ALA) leading to accumulation and formatio
n 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 dysplas
ia (Barrett's esophagus 2, ulcerative colitis 1, Billroth-II stomach 1, rec
tal polyps 2) were treated with oral administration of different concentrat
ions of 5-ALA (10 to 20 mg/kg) or by local instillation of 3 gm 5-ALA in th
e rectum. Endoscopic fluorescence detection was performed 1 to 6 hours afte
r sensitization using a blue light source and compared with conventional wh
ite light endoscopy Biopsies of fluorescent and nonfluorescent areas were c
ompared with histologic findings.
Results: Normal duodenal mucosa and squamous epithelium showed more intense
5-ALA-induced background red fluorescence compared with normal mucosa in t
he stomach or Barrett's mucosa. Histologically, dysplasia was exclusively f
ound in areas with red fluorescence. False-positive fluorescence was associ
ated with microscopic inflammation of the mucosa or feces in the colon.
7Conclusions: 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.