Case Report

Salivary Gland Heterotopia in the Gastroesophageal Junction: A Case Series and Review of the Literature

Table 1

Location, clinical features, endoscopic findings, and histopathology of salivary gland heterotopias at the gastroesophageal junction.

Age/SexLocationClinicalEndoscopyHistopathology

44mGE Junction8 month history of gastro-esophageal reflux disease (GERD).Polypoid shaped, hypoechoic mass measuring 1 cm in size and confined to the deep mucosa and submucosaProminent mucus glands with chronic inflammation consistent with heterotopic salivary glands surrounded by prominent adipose tissue and congested vessels in the submucosa (Figures 1 and 2).

62 mGE JunctionHistory of hypothyroidism, Sjogren’s syndrome, Raynaud syndrome, chronic GERD and grade 3 esophagitisDilated esophagus with an irregular z-line and 2 small islands of salmon colored mucosa immediately proximal to the GE junctionFocal mild acute erosive esophagitis and basal hyperplasia that was consistent with reflux and detached fragment of salivary gland type glandular tissue with chronic inflammation consistent with heterotopic salivary gland tissue (Figures 3 and 4)

72 mGE JunctionPast medical history of Barrett’s esophagus and high-grade dysplasia presented to rule out invasive carcinomaConcerning focal area of ulceration which was removed via EMRFocal high-grade dysplasia, cavernous and ectatic venous channels as well as a few prominent lobules of minor salivary glands with cystification (Figures 5 and 6)