Professional Documents
Culture Documents
Periosteal reaction
The periosteum is not normally visible on a radiograph. The term
‘periosteal reaction’ refers to excess bone produced by the periosteum,
which occurs in response to such conditions as neoplasm, inflammation
or trauma. Several patterns of periosteal reaction are seen, but they do
not correlate with specific diagnoses. At the edge of a very active
periosteal reaction there may be a cuff of new bone known as a
Codman’s triangle Although often seen in highly malignant primary
bone tumours, e.g. osteosarcoma, a Codman’s triangle is also found in
other aggressive conditions.
Cortical thickening
Cortical thickening also involves the laying down of new
bone by the periosteum but here the process is
very slow. The result is that the new bone, although it may
be thick and irregular, shows the same homogeneous
density as does the normal cortex. There are no separate
lines or spicules of calcification as seen in a periosteal reaction. The causes include
chronic osteomyelitis, healed
trauma, response to chronic stress or benign neoplasm. The
feature common to all these conditions is that the process
is either very slowly progressive or has healed.
Causes of osteoporosis
Idiopathic:
– juvenile
– postmenopausal
– senile
• Cushing’s syndrome
• Steroid therapy
• Disuse
Screening for osteoporosis
Because osteoporosis is such a prevalent
problem and, once established, is difficult to
treat, attempts have been made to develop
screening tests for the at-risk population in
order to institute preventative treatment. Bone
mass is usually measured by dual-energy x-ray
absorption, often abbreviated to DEXA.
Rickets and osteomalacia
In these conditions there is poor mineralization of osteoid. If this
occurs before epiphyseal closure, the condition is known as rickets;
in adults the condition is known as osteomalacia.
Causes of rickets and osteomalacia
• Decreased production of endogenous vitamin D:
– dietary deficiency
– lack of exposure to sunlight
• Impaired absorption of calcium or vitamin D:
– malabsorption
• Renal disease, causing vitamin D-resistant rickets, despite
normal amounts of vitamin D in diet:
– tubular defects: hypophosphataemia, Fanconi’s syndrome
and renal tubular acidosis
– chronic renal failure: impaired ability to activate vitamin D
Hyperparathyroidism
Excess parathyroid hormone secretion mobilizes
calcium from the bones, resulting in a decrease
in bone density. Hyperparathyroidism may be
primary, from hyperplasia or a tumour of the
parathyroid glands, or secondary, due to chronic
renal failure .Many patients with primary
hyperparathyroidism present with renal stones
and only a small minority have
radiological bone changes
Generalized increase in bone density
Several conditions can cause a generalized increase in bone
density, including:
• Sclerotic metastases are by far the commonest cause,
particularly from prostatic or breast carcinoma. These may affect
the skeleton diffusely • Osteopetrosis (marble bone disease). In
this congenital disorder of bone formation the bones are densely
sclerotic. The bones are brittle and may fracture readily, but if
fractured they heal easily.
• Myelosclerosis is a form of myelofibrosis in which, in addition
to the replacement of bone marrow by fibrous tissue, the
process extends to lay down extratrabecular bone, usually in a
rather patchy fashion The spleen is invariably enlarged because it
becomes the site of haemopoiesis. It may reach a very large size
and forms an important sign on abdominal radiographs
Alteration of trabecular pattern and change in
shape
Pagets disease
The incidence of Paget’s disease varies greatly from country to
country, being common in the UK but rare in the USA and Asia.
It is usually a chance finding in an elderly patient. One or more
bones may be affected, the usual sites being the pelvis, spine,
skull and long bones. Bone softening causes bowing and
deformity of the bones and pathological fractures may occur.
Hemolytic anaemia
There are several types of haemolytic anaemia, but
radiological changes are seen in two main types: thalassaemia
and sickle cell disease. Both show changes of marrow
hyperplasia, but sickle cell anaemia may also show evidence of
bone infarction and infection.
Changes in bone shape
Bone dysplasias
Bone dysplasias are congenital disorders
resulting in abnormalities in the size and shape
of the bones. There are a large number of
different dysplasias; many of them are
hereditary and all of them are rare.