Clinicopathological features of gastric Langerhans cell histiocytosis and a literature review
Abstract
Objective This study aims to review the clinicopathological features, molecular profiles, and clinical behavior of gastric LCH to increase diagnostic accuracy and improve the understanding of its prognosis. Methods We analyzed five cases of gastric LCH and integrated clinical, endoscopic, and pathological data. Diagnoses were confirmed via immunohistochemistry (S-100, CD1a, and Langerin). BRAF-V600E mutation status was assessed by PCR in three patients. A literature review of 17 additional cases was included for a comprehensive analysis. Results Patients presented with nonspecific symptoms such as abdominal pain. Endoscopy predominantly revealed solitary polyps (
Fields of Study & Subjects
Histiocytic Disorders and Treatments
Gastrointestinal Tumor Research and Treatment
Vascular Malformations and Hemangiomas
Publication details
- Journal / source
- Journal of the Japan Society of the Reticuloendothelial System
- Volume
- 66
- Issue
- 1
- Pages
- 11–18
- Publication date
- 1 January 2026
- Language
- EN