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Variable pathologic interpretation of columnar lined esophagus by general pathologists in community practice
1Department of Medicine, Division of Gastroenterology/Hepatology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Gastrointestinal Endoscopy
|July 1, 1999
Summary
Pathologists show significant disagreement in interpreting columnar lined esophagus biopsies, leading to varied diagnoses of dysplasia and Barrett's esophagus. Expert review is recommended for accurate interpretation of high-grade and low-grade dysplasia.
Area of Science:
- Gastroenterology
- Pathology
- Oncology
Background:
- Accurate pathologic interpretation of columnar lined esophagus is crucial for guiding patient management, including surveillance and surgical decisions.
- This study assesses the consistency of pathologic interpretations of columnar lined esophagus among general pathologists in community practice.
Purpose of the Study:
- To evaluate the interobserver variability in the pathologic interpretation of columnar lined esophagus biopsy specimens by general pathologists.
- To assess the accuracy of diagnosing dysplasia and metaplasia in columnar lined esophagus.
Main Methods:
- Twenty general pathologists reviewed five histologic slides of columnar lined esophagus.
- Cases included intestinal metaplasia with varying degrees of dysplasia (none, low-grade, high-grade) and gastric metaplasia (fundic-type, cardia-type).
Main Results:
- Significant interobserver variation was observed in classifying high-grade dysplasia (identified by 30%) and low-grade dysplasia (identified by 35%).
- Interpretations ranged from no dysplasia to invasive adenocarcinoma, highlighting diagnostic challenges.
- Gastric metaplasia was frequently misidentified as Barrett's esophagus (38% of cases).
Conclusions:
- Pathologic interpretation of columnar lined esophagus by community pathologists exhibits substantial interobserver variability.
- The frequent misapplication of the term Barrett's esophagus for columnar lined esophagus without goblet cells, which lacks clear cancer risk association, suggests reconsidering its use.
- Expert consultation for interpreting high-grade and low-grade dysplasia in esophageal pathology is supported by these findings.