A 16-year-old previously healthy young man presented to the emergency room with fatigue, headaches and pallor. He endorsed a history of black, tarry stool and early satiety for several months. His maternal family history was not significant, and paternal history was unknown. On physical exam, he was pale and was noted to have a systolic flow murmur. There was no organomegaly, and an abdominal mass was not palpable.
Laboratory evaluation was significant for a hemoglobin of 6.6 g/dL with an MCV of 77 fL. The remainder of the CBC was unremarkable, as were electrolytes, hepatic function panel and coagulation studies. Stool guaiac was positive.