Esophageal granular cell tumor: A case report

0Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

BACKGROUND Esophageal granular cell tumor (eGCT) is a relatively rare, usually benign neoplasm of the neuroectoderm. It is derived from Schwann cells. Clinical symptoms of this disease are non-specific. However, the most common presenting symptom is dysphagia, which is mostly misdiagnosed as esophageal polyps under gastroscopy, yet it has a 2% chance of forming cancers. We report the case of a 52-year-old woman with solitary eGCT, then analysed retrospectivelyanalyze the clinical features and elucidate on the reduction of misdiagnosis and missed diagnosis. CASE SUMMARY A 52-year-old woman was diagnosed with “esophageal granulossoma” after esophagoscopy, which was mistaken for eGCT. CONCLUSION eGCT diagnosis depends on characteristic pathomorphologies and detection of the S-100 protein. Endoscopic mucosal resection is the preferred therapeutic method.

Cite

CITATION STYLE

APA

Chen, Y. L., Zhou, J., & Yu, H. L. (2022). Esophageal granular cell tumor: A case report. World Journal of Clinical Cases, 10(19), 6543–6547. https://doi.org/10.12998/wjcc.v10.i19.6543

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free