Match each patient's clinical presentation with the most likely corresponding finding on a peripheral blood smear.
- A 54-year-old asymptomatic man with an incidentally discovered leukocyte count of (predominantly mature-appearing small lymphocytes) and bilateral painless cervical lymphadenopathy.Smudge cells (fragile, disrupted leukocytes)
- A 23-year-old Mediterranean man with lifelong mild, asymptomatic microcytic anemia, normal iron studies, and an elevated hemoglobin fraction.Target cells (codocytes with central hemoglobin concentration)
- A 31-year-old man who develops scleral icterus, dark urine, and a rapid drop in hemoglobin two days after initiating trimethoprim-sulfamethoxazole for a skin infection.Bite cells (degmacytes with semicircular peripheral defects)
- A 72-year-old woman presenting with progressive fatigue, a mean corpuscular volume of , and new-onset loss of vibratory sensation in her lower extremities.Hypersegmented neutrophils (multilobated nuclei)
Answer
Chronic Lymphocytic Leukemia pairs with smudge cells; beta-thalassemia trait pairs with target cells; G6PD deficiency pairs with bite cells; and Vitamin B12 deficiency pairs with hypersegmented neutrophils.
Each peripheral smear finding is generated by a specific mechanism unique to the paired disease: mechanical disruption of fragile B-cells (smudge cells in CLL), relative membrane excess (target cells in thalassemia), splenic macrophage pitting of Heinz bodies (bite cells in G6PD deficiency), and impaired DNA synthesis delaying nuclear lobation (hypersegmented neutrophils in Vitamin B12 deficiency).
Step-by-Step Solution
Key Concept
Peripheral blood smear findings reflect specific underlying pathophysiologic mechanisms in hematologic disorders.
Estimated Time:1m 30s