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Renal Osteodystrophy
· Constellation of musculoskeletal abnormalities occurring with chronic renal failure featuring some combination of o Osteomalacia (adults) o Rickets (children) o 2° hyperparathyroidism o Soft-tissue calcifications o Osteosclerosis o Soft-tissue + vascular calcifications · Low calcium levels lead to osteomalacia o Additional factors responsible for osteomalacia are § Inhibitors to calcification produced in the uremic state § Aluminum toxicity § Dysfunction of hepatic enzyme system A § Renal insufficiency with diminished filtration results in phosphate retention · Maintenance of Ca x P product lowers serum calcium directly, which in turn increases parathyroid hormone production (2°hyperprathyroidsim) · Osteopenia o Combined effect of § Osteomalacia (reduced bone mineralization due to acquired insensitivity to vitamin D / antivitamin D factor) § Osteitis fibrosa cystica (bone resorption) § Osteoporosis (decrease in bone quantity) o Complications § Fracture predisposition (lessened structural strength) with minor trauma · Spontaneously § Fracture prevalence increases with duration of hemodialysis + remains unchanged after renal transplantation · Sites of fractures o Vertebral body (3-25%) o Pubic ramus, rib (5-25%) o Milkman fracture / Looser zones (in 1%) o Metaphyseal fractures o Prognosis § Osteopenia may remain unchanged / worsen after renal transplantation + during hemodialysis · Secondary hyperparathyroidism o Cause § Inability of kidneys to adequately excrete phosphate leads to hyperplasia of parathyroid chief cells (2° hyperparathyroidism) § Excess parathyroid hormone affects the development of osteoclasts, osteoblasts, osteocytes o Hyperphosphatemia o Hypocalcemia o Increased PTH levels o Subperiosteal, cortical, subchondral, trabecular, endosteal, subligamentous bone resorption o Osteoclastoma = brown tumor = osteitis fibrosa cystica (due to parathyroid hormone -stimulated osteoclastic activity § More common in 1° hyperparathyroidism o Periosteal new-bone formation (8-25%) o Chondrocalcinosis § More common in 1° hyperparathyroidism) · Osteosclerosis (9-34%) o One of the most common radiologic manifestations § Most common with chronic glomerulonephritis o May be the sole manifestation of renal osteodystrophy o Diffuse chalky density o Thoracolumbar spine in 60% with dense end-plates produce appearance of rugger-jersey (rugger jersey spine)
Rugger-jersey
spine in o Also in pelvis, ribs, long bones, facial bones, base of skull (children) o Prognosis § May increase/regress after renal transplantation · Soft-tissue calcifications o Metastatic secondary to hyperphosphatemia (solubility product for calcium + phosphate exceeds 60-75 mg/dL in extracellular fluid) § Hypercalcemia § Alkalosis with precipitation of calcium salts o Dystrophic secondary to local tissue injury § Location · Arterial (27-83%) o In medial + intimal elastic tissue § Dorsalis pedis a., forearm, hand, wrist, leg o Pipestem appearance without prominent luminal involvement · Periarticular (0-52%) o Multifocal o Frequently symmetric o May extend into adjacent joint o Chalky fluid / pastelike material o Inflammatory response in surrounding tenosynovial tissue o Discrete cloudlike dense areas § Fluid-fluid level in tumoral calcinosis o Prognosis § Often regresses with treatment · Treatment o Decrease of phosphorus absorption in bowel o Vitamin D3 administration (if vitamin D resistance predominates) o Parathyroidectomy for 3° hyperparathyroidism (= autonomous hyperparathyroidism)
Dahnert 5th edition
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