MKSAP: 63-year-old man with mid-upper back pain


Test your medicine knowledge with the MKSAP challenge, in partnership with the American College of Physicians.

A 63-year-old man is evaluated for severe mid-upper back pain following a minor fall 1 day ago. He also notes progressive fatigue of 6 months’ duration and a 6.8-kg (15-lb) weight loss. Medical history is notable for an 80-pack-year smoking history, although he is currently a nonsmoker.

On physical examination, temperature is 37.3 °C (99.1 °F), blood pressure is 112/74 mm Hg, pulse rate is 98/min, and respiration rate is 18/min. BMI is 22. The cardiopulmonary examination is unremarkable. He has no lymphadenopathy or hepatosplenomegaly. Point tenderness to palpation is noted over the mid thoracic spine. No skin changes or peripheral edema are observed.

Laboratory studies:

Hemoglobin 11 g/dL (110 g/L)
Leukocyte count 4800/µL (4.8 × 109/L) with a normal differential
Platelet count 155,000/µL (155 × 109/L)
Albumin 2.8 g/dL (28 g/L)
Calcium 11.8 mg/dL (3.0 mmol/L)
Creatinine 3.1 mg/dL (274 µmol/L)
Total protein 6.3 g/dL (63 g/L)
Urinalysis Trace protein, no blood, 0 erythrocytes/hpf, no casts
Urine protein-creatinine ratio 2300 mg/g

A chest radiograph shows no infiltrates and a normal cardiac silhouette. Radiographs of the thoracic spine reveal osteopenia with a compression fracture of T6.

Which of the following is the most appropriate diagnostic test to perform next?

A. 1,25-Dihydroxyvitamin D (calcitriol) measurement
B. Intact parathyroid hormone measurement
C. Parathyroid hormone–related protein measurement
D. Serum protein electrophoresis and free light chain test

MKSAP Answer and Critique

The correct answer is D. Serum protein electrophoresis and free light chain test.

Serum protein electrophoresis and serum free light chain (FLC) testing should be performed in this patient with likely multiple myeloma; together, these have a diagnostic sensitivity approaching 100% for multiple myeloma requiring therapy. This patient has several findings suspicious for this disease as the cause of his hypercalcemia, including osteopenia with a thoracic compression fracture, anemia, and kidney dysfunction. However, kidney dysfunction can occur as a direct result of hypercalcemia, regardless of its underlying cause. An important clue in this patient is the discordance between the degree of proteinuria assessed by the urinalysis compared with the urine protein-creatinine ratio. A routine dipstick urinalysis will detect albuminuria but is relatively insensitive at detecting other urine proteins. However, a urine protein-creatinine ratio measures all proteins in the urine, including immunoglobulins, if present. This discrepancy should raise suspicion for monoclonal FLCs in the urine (Bence-Jones proteinuria) and potential cast nephropathy. Similarly, a sulfosalicylic acid test will detect all urine proteins, including light chains, and can be performed for suspected myeloma cast nephropathy. In FLC myeloma, the serum protein electrophoresis may only reveal hypogammaglobulinemia and no monoclonal band or a low-level monoclonal band because of its insensitivity at detecting monoclonal FLCs. However, the serum FLC test, an antibody-based assay that can detect low levels of FLCs, will demonstrate an elevated level of the affected monoclonal FLC and an abnormal serum κ/λ FLC ratio.

Increased 1,25-dihydroxyvitamin D (calcitriol) levels may result from ingestion of calcitriol or increased 25-hydroxyvitamin D (calcidiol) activation to calcitriol as a result of underlying granulomatous disease (for example, sarcoidosis) or lymphoma, thus leading to hypercalcemia.

This patient has no history of calcitriol ingestion and no physical examination or radiographic features of granulomatous disease or lymphoma. Increased calcitriol levels do not explain his anemia, osteopenia and thoracic compression fracture, or kidney dysfunction with nonalbumin proteinuria.

Primary hyperparathyroidism can present with hypercalcemia, bone mineral density loss with increased compression fracture risk, and, when hypercalcemia is severe enough or long-standing, kidney dysfunction. However, primary hyperparathyroidism is uncommonly associated with anemia and does not explain the proteinuria, so measuring the intact parathyroid hormone level is not indicated.

Hypercalcemia associated with myeloma results from osteoclast activation, not secretion of parathyroid hormone–related protein (PTHrP). PTHrP is produced more commonly in solid tumors, such as squamous cell (head and neck, lung); renal cell; and bladder, breast, and ovarian carcinomas. Although the patient has an extensive smoking history, no findings on physical examination or chest radiograph suggest the presence of a solid tumor. Additionally, PTHrP-mediated hypercalcemia from an occult solid tumor would not explain this patient’s proteinuria.

Key Point

  • Combination serum protein electrophoresis and free light chain testing has a sensitivity approaching 100% for diagnosing multiple myeloma requiring therapy.

This content is excerpted from MKSAP 17 with permission from the American College of Physicians (ACP). Use is restricted in the same manner as that defined in the MKSAP 16 Digital license agreement. This material should never be used as a substitute for clinical judgment and does not represent an official position of ACP. All content is licensed to on an “AS IS” basis without any warranty of any nature. The publisher, ACP, shall not be liable for any damage or loss of any kind arising out of or resulting from use of content, regardless of whether such liability is based in tort, contract or otherwise.


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