AI Article Synopsis

  • - Recent studies have debated the link between gastric cancer and negative autoimmune gastritis (AIG), yet this case study presents a 70-year-old woman with gastric cancer who had negative AIG, contradicting earlier notions.
  • - Extensive testing (antibodies, stool antigens, culture, and histology) indicated severe atrophy in her gastric body, associated with high gastrin levels, supporting the AIG diagnosis despite negative results.
  • - The patient developed two cancerous lesions four years later; research suggests that those with advanced gastritis, even with negative AIG, are at increased risk for gastric cancer, highlighting the need for better surveillance and further studies.

Article Abstract

Recent studies have suggested that gastric cancer does not occur in patients with negative autoimmune gastritis (AIG); however, this notion is controversial. We encountered a case of gastric cancer associated with AIG in which infection was excluded. A woman in her 70s was referred to our hospital for endoscopic resection of an antral adenoma. An antibodies test, stool antigens test, culture, and histological analysis using Giemsa staining yielded negative results. AIG was suspected because the antrum was endoscopically normal but the body was severely atrophic, which are typical findings of AIG. Anti-parietal cell antibodies were 40-fold positive, the gastrin level was 2950 pg/ml, and the pepsinogen I level, pepsinogen II level, and pepsinogen I/II ratio were 6.3 ng/ml, 5.7 ng/ml, and 1.1, respectively. A pathological examination of the gastric body revealed severe oxyntic atrophy with hyperplasia of enterochromaffin-like cells, whereas the antrum showed no pyloric gland atrophy or inflammation. These findings indicated that the patient had -negative AIG. Four years later, a depressed lesion in the lower body and a flat lesion at the angle were observed; the former was a poorly cohesive carcinoma, and the latter was a differentiated adenocarcinoma. Surgical resection revealed that the lesion in the lower body was a poorly cohesive carcinoma invading the submucosa with vascular involvement, whereas the lesion in the angle was an intramucosal differentiated adenocarcinoma. A review of previous studies of gastric cancer with -negative AIG suggested that patients with histologically and serologically advanced gastritis are at high risk for carcinogenesis. Even in -negative cases, severe gastric mucosal atrophy in AIG cases may indicate a carcinogenic risk; therefore, surveillance for gastric cancer is especially recommended for these cases. Large cohort studies on the association between -negative AIG and gastric cancer are warranted.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11326753PMC
http://dx.doi.org/10.7759/cureus.66910DOI Listing

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