Chapter 22: Generalized Disease Conditions of Bone

Chapter 22: Generalized
Disease
Conditions of Bone
Soft Tissue Overgrowth
Abnormalities of Alignment
General Increased Bone Density
Osteopenia
Marrow Abnormalities
The Dysplasias
GENERALIZED DISEASE
CONDITIONS OF BONE
Soft Tissue Overgrowth
1. Acromegaly: An acquired condition resulting in excess of growth
hormone due to a pituitary eosinophilic adenoma. Radiographically, it is
characterized by overgrowth of bone, cartilage, and soft tissue. With adult
onset the hands and feet demonstrate the most pronounced skeletal changes
2. Pachydermoperiostosis (Idiopathic Osteoarthropathy): A hereditary

condition transmitted as an autosomal dominant gene. It manifests itself in
adolescence as overgrowth of the soft tissues, periostitis, and synovitis.
Clinically, this is characterized by thickening of the skin, clubbing of the
terminal digits, and painful swollen joints. It does resemble Acromegaly
except the terminal tufts tend to be reabsorbed rather than enlarged. The
scalp demonstrates cutis verticus gyrata-longitudinal wrinkles.
3. Neurofibromatosis-1 (von Recklinghausen's Disease): An autosomal

dominant multisystem disease. Neurofibromas of the skin, bones and. soft
tissues result in grotesque deformities. Neurofibromas occur on the
peripheral and cranial nerves and have the potential for sarcomatous
degeneration. "Cafe-au-lait" spots are present on the skin. Half of these
patients develop skeletal abnormalities which include kyphoscoliosis,
scalloping of the vertebral bodies, rib notching, and a characteristic defect of
the orbit of the eye. The peripheral skeleton can develop overgrowth of the
soft tissues and bones or overtubulation, giving the bones a thin bowed
appearance.
4. Macrodactyly: A localized enlargement of the soft tissues of a digit,

which can be idiopathic or non-idiopathic.
Abnormalities of Alignment
1. Ehlers-Danlos Syndrome: A group of inherited connective tissue
disorders resulting in hyperelasticity of the skin and fragility of blood vessels.
Ligamentous and capsular laxity as well as muscular weakness lead to
subluxation and dislocation. In the feet pes planus is very common. Atrophic
scarring occurs: There are 9 subtypes. Types I, II, and III are the most
common, and are autosomal dominant types.
2. Marfan's Syndrome: An inherited autosomal dominant connective tissue

disorder resulting in abnormal elastic tissue and collagen production and
excessive laxity. Hyperextensible joints and ligamentous laxity result in
hallux valgus and pes planus, and kyphoscoliosis. The most serious
complication of Marfan's syndrome is a dissecting aneurysm of the aorta.
The radiographic hallmark of Marfan's is exaggerated length of the bones.
The lens of the eye Is also displaced usually upward.
General Increased Bone Density
1. Osteopetrosis (Albers-Schonberg Disease): An inherited bone disease
causing diffusely dense bones. The basic defect is a failure of osteoclasts to
absorb primary spongiosa during enchondral bone formation. This leads to a
"bone-within-a-bone" appearance. The bone is actually very weak.
2. Melorrheostosis: An acquired condition causing cortical thickening. Its

etiology is unknown. The cortical thickening is smooth and thick and involves
the periosteal surface or the endosteal surface, encroaching on the medullary
canal.
3. Osteopoikilosis: A hereditary "spotted" bone disorder transmitted as an

autosomal dominant. There are multiple round or oval bone densities
occurring in the spongiosa of bone. There is a predilection for the tarsus in
the foot. There is no uptake with this via bone scan (differential for blastic
metastases).
4. Bone Islands: Are histologically identical to osteopoikilosis but occur as

single lesions.
5. Paget's Disease of Bone: The destruction of bone with subsequent

repair results in thickened, disorganized trabeculae and increased size of
bone, giving the appearance of increased density. Usually the tibia is
affected, but can involve the bones of the feet. The coarse trabeculae often
have a different appearance from blastic metastases and melorrheostosis.
Malignant degeneration is a rare complication (malignant fibrous
histiocytoma, osteosarcoma, fibrosarcome, chondrosarcoma-all called
"Paget's sarcoma" if they occur in a setting of Paget's Disease of Bone).
Osteopenia
1. Rickets and Osteomalacia: Due to deficient mineralization of bone
specifically due to insufficient vitamin D from malabsorption, renal disease,
lack of adequate sunlight, liver disease, and metabolic disorders. In the child
this can cause widening of the growth plate, cupping of the epiphyses, and
bowing of the legs. The pathognomonic sign of osteomalacia is the presence
of Looser's lines or pseudofractures. These lucent lines are perpendicular to
the cortex, are often bilateral and symmetrical.
2. Osteoporosis (decreased bone mass): Loss of trabeculae and thinning

of the cortex
i. Scurvy: Lack of vitamin C results in failure to produce intracellular
substances, therefore, osteoporosis of the adjacent metaphysis, seen as a
transverse radiolucent bands. This is called the scurvy line. Fractures can
occur through this zone with complete separation of the epiphyseal plate.
The vascular endothelium is abnormal, which leads to hemorrhage.
Subperiosteal bleeding causes wide separation of the periosteum, and
healing manifests as a thin shell of peripheral periosteal new bone. It takes a
minimum of 4 months of lack of vitamin C for the disease to become
apparent. This is very rare today in developed countries.
ii. Osteogenesis Imperfecta (Ekman-Lobstein disease): A generalized

connective tissue disorder that is inherited as an autosomal dominant gene.
A deficiency of osteoblasts results in severe generalized osteoporosis, the
long bones are overtrabeculated and bowed, and protrusio acetabuli are
frequently seen. Additionally there is abnormal dentition, blue sclerae and
early deafness.
iii. Disuse: Diffuse, severe osteoporosis accompanies disuse or

immobilization, with changes resulting in thinning of the cortex and loss of
trabeculae giving the bone a ground glass appearance.
iv. Reflex Sympathetic Dystrophy Syndrome (Sudek's Atrophy):

Generally follows minor trauma, with severe pain and soft tissue swelling and
rapid demineralization. Rapid loss of mineral results in a patchy"motheaten"
pattern of demineralization. (see Chapter: Neurology).
The basic radiological changes inherent to all the marrow affecting

disorders includes expansion of the marrow cavity, thinning of the
trabeculae, and the appearance of rectangular, osteopenic bone.
Marrow Abnormalities
1. Anemias:
i. Thalassemia major: causes microcytic/hypochromic anemia. Generalized
involvement of all the bones of the feet occurs as mentioned above.
ii. Sickle cell disease: produces changes similar to thalassemia. Those
changes can sometimes be mistaken for osteomyelitis. Can cause infarctions
in bone due to vascular blockage by abnormal RBC's.
2. Storage Diseases:
i. Glycogen storage diseases (Von Gierke's disease)
ii. Cerebrosides (Gaucher's disease and Niemann-Pick disease)
iii. Mucopolysaccharides (Hurler's, Hunter's, Sanfiiippo's. Morquio's,
Scheie's, and Maroteaux-Lamy syndromes)
3. Fibro-Osseous Dysplasia:
i. Fibrous dysplasia: A developmental anomaly that results in fibrous tissue
replacement of the marrow cavity
4. Granulomatous Diseases:
i. Sarcoidosis: a systemic granulomatous disease of unknown etiology that
can affect the bones in a small percentage of cases, and when involved,
almost always is seen in the phalanges causing small punched-out defects.
Severe involvement may result in cortical destruction, fractures, and collapse
of bone, giving an arthritis mutilans scenario.
ii. Tuberculosis: Granulomatous disease due to hematogenous spread of
the TB bacillus. Acid fast stains show TB bacilli, which are not seen in Sarcoid.
5. Infarction: Any type of vascular obstruction may result in marrow

infarction. The radiographic changes are frequently those of bone
destruction.
i. Pancreatic disease
Dysplasia is a disturbance in the formation and modeling of bone; it is usually

hereditary and most commonly occurs as a result of inborn errors in
metabolism. Foot dysplasias are an expression of a generalized skeletal
anomaly.
The Dysplasias
1. Spondyloepiphyseal Dysplasia (Morquio-Brailsford disease)
2. Multiple Epiphyseal Displasia (Fairbank's disease)
3. Chondrodysplasia punctata (Conradi's disease)
The Occurence of Cone Shaped Epiphyses

a. Normal variant
b. Chondroectodermal dysplasia (Ellis-van Crevald syndrome)
c. Cleidocranial dysostosis
d. Dyschondrosteosis
e. Hand-foot-uterus syndrome
f. Oto-palato-digital syndrome
g. Osteopetrosis
h. Pycnodysostosis
i. Tricorhinophalangeal syndrome
Occurence of Polydactyly
a. Arthrogryphosis
b. Basal cell of
Occurence nevus syndrome
Tarsal Coalition
c.
a. Cleidocranial dyostosis
Isolated variant (usually in the hindfoot)
d.
b. Ellis-van Crevald syndrome
Juvenile rheumatoid arthritis
e. Gorlin-Chaudhry-Moss
c. Apert's syndrome syndrome
f.
d. Larsen's syndrome
Arthrogryphosis multiplex congenita
g. Myositis ossificanssyndrome
e. Hand-foot-uterus progressiva
h. Rubenstein-Taybi syndrome
f. Oto-palato-digital syndrome (Taybi's syndrome)
i. Trisomy 13-15 (Perth's syndrome)
Occurence of Short Hallux
Occurence of Syndactyly
a. Myositis ossificans progressiva
a. Normal variant
b. Taybi's syndrome
b. Apert's syndrome
c. Hand-foot-uterus syndrome
c. Carpenter's syndrome
d. Apert's syndrome
d. Bloom's syndrome
e. Larsen's syndrome
e. Down's syndrome
f. Popliteal pterygium syndrome
f. F syndrome
g. Franconi's syndrome
g. Laurence-Moon-Biedl syndrome
h. Holt Oram's syndrome
h. Taybi's syndrome
i. Popliteal pterygium syndrome
j. Prader-Willi syndrome
k. Silver's syndrome
l. Trisomy 13
Occurence of Short Metatarsals

a. Normal variant
b. Enchondromatosis
c. Juvenile RA
d. Osteochondromatosis
e. Pseudohypoparathyroidism
f. Pseudopseudohypoparathyroidism
g. Trauma
h. Turner's syndrome*
*Turner's syndrome is-one of the more common chromosomal syndromes

resulting in a sex chromosome" abnormality that causes a XO pattern.
Important clinical findings are coarctation of the aorta, horseshoe kidneys,
short neck, and hypogonadism. Radiographically, a short 4th metatarsal is
commonly found.

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Chapter 22: Generalized

2. Pachydermoperiostosis (Idiopathic Osteoarthropathy): A hereditary

3. Neurofibromatosis-1 (von Recklinghausen's Disease): An autosomal

4. Macrodactyly: A localized enlargement of the soft tissues of a digit,

2. Marfan's Syndrome: An inherited autosomal dominant connective tissue

2. Melorrheostosis: An acquired condition causing cortical thickening. Its

3. Osteopoikilosis: A hereditary "spotted" bone disorder transmitted as an

4. Bone Islands: Are histologically identical to osteopoikilosis but occur as

5. Paget's Disease of Bone: The destruction of bone with subsequent

2. Osteoporosis (decreased bone mass): Loss of trabeculae and thinning

ii. Osteogenesis Imperfecta (Ekman-Lobstein disease): A generalized

iii. Disuse: Diffuse, severe osteoporosis accompanies disuse or

iv. Reflex Sympathetic Dystrophy Syndrome (Sudek's Atrophy):

The basic radiological changes inherent to all the marrow affecting

5. Infarction: Any type of vascular obstruction may result in marrow

Dysplasia is a disturbance in the formation and modeling of bone; it is usually

The Occurence of Cone Shaped Epiphyses

Occurence of Short Metatarsals

*Turner's syndrome is-one of the more common chromosomal syndromes

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