S6413 Autoimmune Metaplastic Atrophic Gastritis Presenting With Vitamin B12 Deficiency, Pancytopenia, and Gastric Neuroendocrine Tumor

Introduction: Autoimmune metaplastic atrophic gastritis (AMAG) is a chronic immune-mediated disorder causing oxyntic mucosal atrophy, achlorhydria, and hypergastrinemia, predisposing to neuroendocrine tumors (NETs). The progression of AMAG and vitamin B12 deficiency to NET is a rare presentation. Case Description/Methods: A 52-year-old man with hypertension and diabetes presented with epigastric discomfort, worsened with food intake, and associated with bloating for 10 years. Despite prior repeated triple therapy and PPI for Helicobacter pylori positive gastritis, symptoms only partially improved and relapsed and persisted. Initial evaluation revealed severe vitamin B12 deficiency (98.21 pg/mL) and pancytopenia. A bone marrow biopsy confirmed megaloblastic erythropoiesis, which resolved after parenteral vitamin B12 administration. Endoscopy with biopsy showed AMAG with intestinal metaplasia and a 1.5 cm gastric NET (grade II, Pan-cytokeratin, synaptophysin, and chromogranin A positive, and Ki-67 3%-5%). Elevated gastrin (384 pg/mL) and anti-parietal cell antibodies (1:20) were detected. Partial gastrectomy was planned due to tumor size, grade II histology, and lack of local endoscopic expertise for submucosal dissection. Post-surgery, parenteral vitamin B12 levels were maintained at 1401 pg/ml, with normalization of hematologic parameters. The patient is asymptomatic after surgery. Discussion: This case highlights AMAG as a critical differential in refractory dyspepsia with cytopenias. Chronic hypergastrinemia in AMAG necessitates surveillance for NETs due to its role in ECL cell hyperplasia and tumorigenesis, particularly in high-risk patients (age >50 years, long-standing disease). Surgical management remains pivotal for larger, more aggressive NETs in resource-limited settings. Multidisciplinary care, including vitamin B12 monitoring and tailored oncologic intervention, optimizes outcomes.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001154112.03813.4a
Primary Topic
Helicobacter pylori-related gastroenterology studies
Type
article
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article

S6413 Autoimmune Metaplastic Atrophic Gastritis Presenting With Vitamin B12 Deficiency, Pancytopenia, and Gastric Neuroendocrine Tumor

Mohan Khadka, Samjhana Belbase, Ramesh Bhandari, P Thapa et al.
The American Journal of Gastroenterology
Helicobacter pylori-related gastroenterology studies
article

S6413 Autoimmune Metaplastic Atrophic Gastritis Presenting With Vitamin B12 Deficiency, Pancytopenia, and Gastric Neuroendocrine Tumor

Mohan Khadka, Samjhana Belbase, Ramesh Bhandari, P Thapa, Bal Man Singh Karki
article en

Abstract

Introduction: Autoimmune metaplastic atrophic gastritis (AMAG) is a chronic immune-mediated disorder causing oxyntic mucosal atrophy, achlorhydria, and hypergastrinemia, predisposing to neuroendocrine tumors (NETs). The progression of AMAG and vitamin B12 deficiency to NET is a rare presentation. Case Description/Methods: A 52-year-old man with hypertension and diabetes presented with epigastric discomfort, worsened with food intake, and associated with bloating for 10 years. Despite prior repeated triple therapy and PPI for Helicobacter pylori positive gastritis, symptoms only partially improved and relapsed and persisted. Initial evaluation revealed severe vitamin B12 deficiency (98.21 pg/mL) and pancytopenia. A bone marrow biopsy confirmed megaloblastic erythropoiesis, which resolved after parenteral vitamin B12 administration. Endoscopy with biopsy showed AMAG with intestinal metaplasia and a 1.5 cm gastric NET (grade II, Pan-cytokeratin, synaptophysin, and chromogranin A positive, and Ki-67 3%-5%). Elevated gastrin (384 pg/mL) and anti-parietal cell antibodies (1:20) were detected. Partial gastrectomy was planned due to tumor size, grade II histology, and lack of local endoscopic expertise for submucosal dissection. Post-surgery, parenteral vitamin B12 levels were maintained at 1401 pg/ml, with normalization of hematologic parameters. The patient is asymptomatic after surgery. Discussion: This case highlights AMAG as a critical differential in refractory dyspepsia with cytopenias. Chronic hypergastrinemia in AMAG necessitates surveillance for NETs due to its role in ECL cell hyperplasia and tumorigenesis, particularly in high-risk patients (age >50 years, long-standing disease). Surgical management remains pivotal for larger, more aggressive NETs in resource-limited settings. Multidisciplinary care, including vitamin B12 monitoring and tailored oncologic intervention, optimizes outcomes.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Helicobacter pylori-related gastroenterology studies
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S6413 Autoimmune Metaplastic Atrophic Gastritis Presenting With Vitamin B12 Deficiency, Pancytopenia, and Gastric Neuroendocrine Tumor — Mohan Khadka, Samjhana Belbase, et al. · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS