| Osteomalacia (rickets) |
| Classification and external resources |
| ICD-10 |
M83 |
| ICD-9 |
268.2 |
| DiseasesDB |
9351 |
| MedlinePlus |
000376 |
| eMedicine |
ped/2014 radio/610 |
| MeSH |
D010018 |
Osteomalacia is the softening of the bones caused by defective bone mineralization secondary to inadequate amounts of available phosphorus and calcium, or because of overactive resorption of calcium from the bone as a result of hyperparathyroidism (which causes hypercalcemia, in contrast to other aetiologies).[1] Osteomalacia in children is known as rickets, and because of this, use of the term osteomalacia is often restricted to the milder, adult form of the disease. It may show signs as diffuse body pains, muscle weakness, and fragility of the bones. The most common cause of the disease is a deficiency in vitamin D, which is normally obtained from the diet and/or from sunlight exposure.[2]
Contents
- 1 General characteristics
- 2 Causes
- 3 Signs and Symptoms
- 4 Clinical features
- 5 Biochemical findings
- 6 Radiographic characteristics
- 7 Treatment
- 8 References
- 9 See also
General characteristics
Osteomalacia is a generalized bone condition in which there is inadequate mineralization of the bone. Many of the effects of the disease overlap with the more common osteoporosis, but the two diseases are significantly different. There are two main causes of osteomalacia: (1) insufficient calcium absorption from the intestine because of lack of dietary calcium or a deficiency of, or resistance to, the action of vitamin D; and (2) phosphate deficiency caused by increased renal losses.
Osteomalacia is derived from Greek: osteo- which means "bone", and malacia which means "softness". In the past, the disease was also known as malacosteon and its Latin-derived equivalent, mollities ossium.
Causes
The causes of adult osteomalacia are varied, but ultimately result in a vitamin D deficiency:
- Insufficient nutritional quantities or faulty metabolism of vitamin D or phosphorus
- Renal tubular acidosis
- Malnutrition during pregnancy
- Malabsorption syndrome
- Hypophosphatemia[3]
- Chronic renal failure
- Tumor-induced osteomalacia
- Long-term anticonvulsant therapy[4]
- Coeliac disease[5]
- Cadmium poisoning, Itai-itai disease
Signs and Symptoms
- Weak bones
- Bone pain
- Spinal bone pain
- Pelvic bone pain
- Leg bone pain
- Muscle weakness
- Hypocalcemia
- Compressed vertebrae
- Pelvic flattening
- Easy fracturing
- Bone softening
- Bending of bones
Clinical features
Osteomalacia in adults starts insidiously as aches and pains in the lumbar (lower back) region and thighs, spreading later to the arms and ribs. The pain is symmetrical, non-radiating and is accompanied by sensitivity in the involved bones. Proximal muscles are weak, and there is difficulty in climbing up stairs and getting up from a squatting position.
Due to demineralization bones become less rigid. Physical signs include deformities like triradiate pelvis[6] and lordosis. The patient has a typical "waddling" gait. However, those physical signs may derive from a previous osteomalacial state, since bones do not regain their original shape after they become deformed.
Pathologic fractures due to weight bearing may develop. Most of the time, the only alleged symptom is chronic fatigue, while bone aches are not spontaneous but only revealed by pressure or shocks.
It differs from renal osteodystrophy, where the latter shows hyperphosphatemia.
Biochemical findings
Biochemical features are similar to those of rickets. The major factor is an abnormally low vitamin D concentration in blood serum.
Major typical biochemical findings are given below:
- The serum calcium is low
- Urinary calcium is low
- Serum phosphate is low except in cases of renal osteodystrophy
- Serum alkaline phosphatase is high
Furthermore, a technetium bone scan will show increased activity.
Comparison of bone pathology
|
Condition |
Calcium |
Phosphate |
Alkaline phosphatase |
Parathyroid hormone |
Comments |
| Osteoporosis |
unaffected |
unaffected |
normal |
unaffected |
decreased bone mass |
| Osteopetrosis |
unaffected |
unaffected |
elevated |
unaffected |
thick dense bones also known as marble bone |
| Osteomalacia and rickets |
decreased |
decreased |
elevated |
elevated |
soft bones |
| Osteitis fibrosa cystica |
elevated |
decreased |
elevated |
elevated |
brown tumors |
| Paget's disease of bone |
unaffected |
unaffected |
variable (depending on stage of disease) |
unaffected |
abnormal bone architecture |
Radiographic characteristics
Radiological appearances include:
- Pseudofractures, also called Looser's zones.
- Protrusio acetabuli, a hip joint disorder
Treatment
Nutritional osteomalacia responds well to administration of 10,000 IU weekly of vitamin D for four to six weeks. Osteomalacia due to malabsorption may require treatment by injection or daily oral dosing[7] of significant amounts of vitamin D.
References
- ^ TheFreeDictionary > osteomalacia Citing: Mosby's Medical Dictionary, 8th edition. Copyright 2009
- ^ MedlinePlus Medical Encyclopedia: Osteomalacia
- ^ "Autoimmunity research foundation, Science behind Vitamin D". Retrieved 2011-07-19.
- ^ Pack, Alison (2008). "Bone health in people with epilepsy: is it impaired and what are the risk factors". Seizure 17 (2): 181–6. doi:10.1016/j.seizure.2007.11.020. PMID 18187347.
- ^ Albany, Costantine; Servetnyk, Zhanna (2009). "Disabling osteomalacia and myopathy as the only presenting features of celiac disease: a case report". Cases Journal 2 (1): 20. doi:10.1186/1757-1626-2-20. PMC 2626577. PMID 19128487.
- ^ Chakravorty, N. K. (1980). "Triradiate deformity of the pelvis in Paget's disease of bone.". Postgraduate Medical Journal 56 (653): 213–5. doi:10.1136/pgmj.56.653.213. PMC 2425842. PMID 7393817.
- ^ Eisman, John A. (1988). "6 Osteomalacia". Baillière's Clinical Endocrinology and Metabolism 2: 125–55. doi:10.1016/S0950-351X(88)80011-9.
See also
- Osteopetrosis, the opposite of osteomalacia
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Malnutrition or Nutrition disorders (E40–E68, 260–269)
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| Undernutrition |
Protein-energy
malnutrition |
- Kwashiorkor
- Marasmus
- Catabolysis
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| Avitaminosis |
| B vitamins |
- B1: Beriberi / Wernicke–Korsakoff syndrome (Wernicke's encephalopathy
- Korsakoff's syndrome)
- B2: Ariboflavinosis
- B3: Pellagra (Niacin deficiency)
- B6: Pyridoxine deficiency
- B7: Biotin deficiency
- B9: Folate deficiency
- B12: Vitamin B12 deficiency
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Other
vitamins |
- A: Vitamin A deficiency/Bitot's spots
- C: Scurvy
- D: Hypovitaminosis D/Rickets/Osteomalacia
- E: Vitamin E deficiency
- K: Vitamin K deficiency
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Mineral
deficiency |
- Sodium
- Potassium
- Magnesium
- Calcium
- Iron
- Zinc
- Manganese
- Copper
- Iodine
- Chromium
- Molybdenum
- Selenium (Keshan disease)
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| Overnutrition |
| Overweight
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- Childhood obesity
- Obesity hypoventilation syndrome
- Abdominal obesity
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| Vitamin poisoning |
- Hypervitaminosis A
- Hypervitaminosis D
- Hypervitaminosis E
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| Mineral overload |
- see inborn errors of metal metabolism, toxicity
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noco, nuvi, sysi/epon, met
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Osteochondropathy (M80–M94, 730–733)
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| Osteopathies |
| Osteitis |
| endocrine bone disease: |
|
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| infectious bone disease: |
- Osteomyelitis
- Sesamoiditis
- Brodie abscess
- Periostitis
- Vertebral osteomyelitis
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Bone density
and structure |
| Density / metabolic bone disease |
- Osteoporosis
- Osteopenia
- Osteomalacia
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| Continuity of bone |
- Pseudarthrosis
- Stress fracture
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| Other |
- Fibrous dysplasia
- Skeletal fluorosis
- bone cyst
- Hyperostosis
- Infantile cortical hyperostosis
- Osteosclerosis
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| Bone resorption |
- Osteolysis
- Hajdu-Cheney syndrome
- Ainhum
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| Ischemia |
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| Other |
- Paget's disease of bone
- Algoneurodystrophy
- Hypertrophic pulmonary osteoarthropathy
- Nonossifying fibroma
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| Chondropathies |
|
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| Both |
| Osteochondritis |
- Osteochondritis dissecans
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| Juvenile osteochondrosis |
| leg: |
- hip
- Legg–Calvé–Perthes syndrome
- tibia
- Osgood-Schlatter disease
- Blount's disease
- foot
- Köhler disease
- Sever's disease
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| spine |
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| arm: |
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anat (c/f/k/f, u, t/p, l)/phys/devp/cell
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noco/cong/tumr, sysi/epon, injr
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