Match each patient's clinical presentation with the most appropriate targeted laboratory evaluation panel to establish the diagnosis.
- A 65-year-old man is found to have an isolated, asymptomatic elevation of total serum protein with a normal albumin level and normal complete blood count during a routine wellness examination.Serum protein electrophoresis, serum immunofixation, and serum free light chain assay
- A 32-year-old woman is evaluated for an unprovoked deep vein thrombosis in her left lower extremity. She has a past medical history significant for two consecutive second-trimester pregnancy losses.Lupus anticoagulant, anticardiolipin antibodies, and anti-beta-2-glycoprotein I antibodies
- A 48-year-old woman presents with progressive fatigue, symmetrical paresthesias in her lower extremities, a smooth and beefy-red tongue, and macrocytic anemia on complete blood count.Serum vitamin B12, methylmalonic acid, and homocysteine levels
- A 25-year-old man of Mediterranean descent presents for evaluation of lifelong microcytic anemia. Previous trials of oral iron supplementation have not improved his hemoglobin levels, and his serum ferritin is normal.Hemoglobin electrophoresis or high-performance liquid chromatography (HPLC)
Answer
The correct matches align the protein gap with electrophoresis, the unprovoked thrombosis/miscarriages with antiphospholipid antibodies, the macrocytic anemia/neuropathy with B12 testing, and the iron-refractory microcytic anemia with hemoglobin electrophoresis.
Each clinical vignette provides classic diagnostic clues for distinct hematologic disorders. A protein gap indicates a potential plasma cell dyscrasia. Thrombosis with pregnancy loss characterizes antiphospholipid syndrome. Macrocytosis with neuropathy is the hallmark of B12 deficiency. Microcytosis with normal iron stores in a Mediterranean patient is typical of beta-thalassemia trait.
Step-by-Step Solution
Key Concept
Appropriate targeted laboratory testing based on clinical vignettes of common hematologic disorders.