INTRODUCTION: Collagenous gastritis (CG) is a rare disease characterized by subepithelial deposition of collagen bands and infiltration of inflammatory mononuclear cells in the lamina propria. Since 1989, there have been approximately 100 reported cases, limiting understanding of disease management. We discuss a 55-year-old female in the hopes of providing more information regarding CG. CASE DESCRIPTION/METHODS: A 55-year-old Caucasian female with a history of hypothyroidism presented with a 6-month history of diarrhea, epigastric pain, and loss of appetite. The patient stated stools were up to 5 times a day; epigastric pain was described as a burning sensation. She was on a short course of antibiotics for an upper respiratory tract infection 2 months prior. C. difficile, stool culture, and stool white blood cell were collected and were negative. Bloodwork was obtained including CBC, CMP, lipids, TSH, vitamin D, and HbA1c and were within normal limits. The patient was referred to gastroenterology. Abdominal ultrasound was performed and noted no sonographic abnormality of the abdomen. EGD showed localized continuous petechiae of the antral mucosa; abnormal vascularity, as well as petechiae and scarring of the mucosa of the stomach body (Figure 1). Colonoscopy demonstrated moderate diverticulosis of the left side of the colon (Figure 2). Biopsies were performed of the duodenum, stomach body, rectal polyp, and colon. Immunohistochemical stain was negative for H. pylori. Biopsies of the colon and rectal polyp confirmed collagenous colitis. Gastric biopsy demonstrated impressive full thickness lamina propria dense fibrosis, mixed chronic inflammation, complete gland atrophy, metaplastic mucous glands, epithelial injury, necroinflammatory luminal debris, and intraepithelial neutrophils. Trichrome stain was performed that highlighted marked collagen deposition, confirming our diagnosis of collagenous gastritis. HHV8 immunohistochemical stain of gastric biopsy was completed, to exclude Kaposi sarcoma, and was negative. The patient was successfully initiated on 1 gram of sucralfate four times a day. DISCUSSION: CG is a rare disease, previous case reports have enabled physicians to characterize biopsy findings and we aim to add to that pool. No trials have been conducted with regards to treatment, therefore we hope our patient’s may be useful for physicians researching treatment strategies for both current and future patients.Figure 1.: Stomach Body Scarring and Petechiae.Figure 2.: Descending Colon Diverticulosis.