A hospital laboratory is reviewing several distinct metabolic profiles of patients with disorders of calcium homeostasis. Match each patient's serum and urine biochemical profile to the most likely underlying pathophysiological mechanism.
- Elevated serum , decreased serum , elevated intact PTH, and elevated 24-hour urinary calciumAutonomous hormone secretion from a monoclonal chief cell adenoma
- Decreased serum , elevated serum , elevated intact PTH, and decreased 1,25-dihydroxycholecalciferolImpaired renal phosphate clearance and compromised 1-alpha-hydroxylase activity
- Elevated serum , high-normal intact PTH, and decreased fractional excretion of calcium (< 1%)Inactivating mutation of the G-protein coupled calcium-sensing receptor
- Elevated serum , high-normal serum , suppressed intact PTH, and elevated 1,25-dihydroxycholecalciferolEctopic, unregulated 1-alpha-hydroxylase activity by activated macrophages
- Decreased serum , elevated serum , suppressed intact PTH, and decreased 1,25-dihydroxycholecalciferolAcquired or autoimmune absence of functioning parathyroid glandular tissue
Cevap
Profile 1 matches autonomous adenoma; Profile 2 matches impaired renal clearance; Profile 3 matches CaSR mutation; Profile 4 matches ectopic macrophage activity; Profile 5 matches absent parathyroid tissue.
Each laboratory profile uniquely matches a specific pathophysiological lesion. The interplay between calcium, phosphorus, PTH, and vitamin D allows for precise localization of the defect to the parathyroid glands, kidneys, calcium-sensing receptors, or ectopic sources.
Adım Adım Çözüm
Anahtar Kavram
Differential diagnosis of calcium and phosphate homeostasis disorders based on the parathyroid hormone, 1,25-dihydroxyvitamin D, and urinary calcium axes.