Gastric Fundic Gland Adenocarcinoma With Chief Cell Differentiation

Abstract

A previously healthy sixty-six year old Caucasian man was referred for an outpatient upper endoscopy and colonoscopy for mild iron deficiency anemia. He had episodic heartburn for which he occasionally took calcium carbonate. He denied any weight loss. His family history was positive for colon cancer in his mother at age 74. He had a twenty pack year tobacco history but quit one year ago. His colonoscopy identified two small tubular adenomas. On upper endoscopy, his esophagus and duodenum appeared normal. On retroflexion in the stomach, there was an irregular 7mm erythematous polypoid lesion in the fundus (Figure 1). Image enhanced endoscopy with narrow band imaging identified increased vascularity and a gyrus-like mucosal pit pattern (Figure 2). Band EMR was performed after initial biopsy revealed dysplasia and the polypoid lesion was removed en bloc. Histologic examination (hematoxylin and eosin stain, Figure 3) revealed well-differentiated gastric adenocarcinoma with chief cell differentiation arising from oxyntic mucosa and invading into the superficial submucosa (arrows). Mucosal and deep resection margins were clear of carcinoma and there was no lymphovascular or perineural invasion. The patient did well post procedure and will undergo a repeat upper endoscopy within six months. Figure 1 Figure 2 Figure 3 While gastric adenocarcinoma is not an uncommon cancer worldwide, gastric adenocarcinoma with chief cell differentiation is a recently described rare epithelial neoplasm of the stomach with unique clinicopathologic characteristics. Unlike conventional types of gastric adenocarcinoma, which typically present with advanced, including metastatic, disease, gastric adenocarcinoma with chief cell differentiation may be a locally curable entity. The initial description in the literature was a case series of twelve Japanese patients.1 More recently, a second case series identified ten additional patients, two of whom were Caucasian.2 Like our patient, all reported patients to date had a solitary polyp, and in the majority, the polyp was located in the gastric fundus. Invasion limited to the submucosa was seen in the initial case series in the majority of patients, but was not identified in the second series, although in that study, specimens examined were superficial biopsy samples only and the submucosa was not evaluated. In both studies, none of the patients developed tumor recurrence or metastasis, leading authors to question if the term oxyntic gland polyp is more appropriate for this lesion, rather than gastric adenocarcinoma with chief cell differentiation. Regardless of the nomenclature, our case highlights that this rare variant of gastric adenocarcinoma may occur in non-Asian patients and emphasizes the utility of narrow band imaging and the importance of endoscopic mucosal resection, given the possibility of submucosal invasion and the ability to achieve curative resection of this rare and unique type of gastric neoplasm.