An 87-year-old man was referred to our institution because of a 4-month history of progressive fatigue and orthostatic symptoms. Mild anemia (hemoglobin concentration, 11.1 g/dL) was noted 4 months before the onset of symptoms, but his hemoglobin concentration (14.0 g/ dL) was normal 15 months before that. He had no episodes of syncope but noticed poor exercise tolerance, making it difficult to continue bowling, his favorite pastime. No change was noted in appetite or weight, and he experienced no fever, chills, cough, chest pain, shortness of breath, palpitations, abdominal pain, or altered bowel pattern. The patient had no history of recurrent infections and was not aware of excessive bruising or any source of blood loss, particularly from the gastrointestinal or genitourinary tract. There was no history of recent blood transfusions, but he had taken iron supplements for a few weeks 1 year before presentation and continued to take a daily oral multivitamin with iron since that time. He denied taking any other medications. His medical history included sensorineural hearing loss, Gilbert disease, mild dependent edema, and diverticulosis coli. Physical examination revealed pronounced pallor. Orthostatic hypotension was noted, with an increase in his pulse rate from 62/min to 75/min and a decrease in systolic blood pressure from 120 mm Hg to 104 mm Hg from lying down to standing. The patient had no evidence of oropharyngeal abnormalities, excessive bruising, petechiae, lymphadenopathy, hepatosplenomegaly, or neuropathy. A trace of pitting edema was evident bilaterally on his lower extremities. Initial laboratory studies (reference ranges shown parenthetically) revealed a hemoglobin level of 6.9 g/dL (13.517.5 g/dL), mean corpuscular volume (MCV) of 115.6 fL (81.2-95.1 fL), leukocyte count of 4.3 × 10/L (3.5-10.5 × 10/L) with a normal leukocyte differential, and platelet count of 261 × 10/L (150-450 × 10/L) determined by an automated hematology analyzer.