Terminal ileum hemosiderosis secondary to prolonged oral iron ingestion

Abstract

A 74-year-old Asian woman was referred for outpatient upper and lower endoscopic screening. She had history of hyperlipidemia and vegetarianism. Her medications included atorvastatin and self-medication of oral iron for the last 10 years. Routine blood tests were normal. Esophagogastroduodenoscopy was macroscopically and histologically normal. Colonoscopy disclosed diffuse brownish tiny spots of the mucosa of the terminal ileum (Fig. 1). Biopsy specimens showed pigment deposition at the level of the lamina propria (Fig. 2). A positive iron stain indicated hemosiderin deposition. Retrospective review of the patient’s medical archives over the last 16 years revealed normal iron studies without any signs of iron deficiency anemia, hemolysis or hemochromatosis. She was consequently asked to discontinue iron supplements. Figure 1 (A) Pigmented mucosa of the terminal ileum as seen by white light and (B) narrow-band imaging Figure 2 (A) Histology revealed brown pigment deposition within macrophages in lamina propria of normal villi (Hematoxylin-Eosin, 40x) (B) Positive Prussian blue stain suggesting hemosiderosis (40x) Hemosiderosis of the gastrointestinal tract is usually associated with hemochromatosis, chronic renal failure, diabetes, oral or parenteral iron therapy, multiple blood transfusions and several antihypertensive medications (primary hydralazine and furosemide). It has been described to affect the whole gastrointestinal tract, with the duodenum reported as the most common extracolonic site. A PubMed research revealed only 5 case reports of hemosiderosis isolated to the terminal ileum, associated with chronic oral iron intake (2 cases) and/or chronic renal failure (2 cases) or hemochromatosis (1 case) [1-3]. Gastroenterologists should be aware of this rare endoscopic entity and its association with long-term iron supplementation to avoid unnecessary further investigation.