Thalassemia
Updates to Article Attributes
Thalassaemia is an autosomal recessive haemoglobinopathy first described in the Mediterranean region. The genetic defect causes a reduction in the rate of globin chain synthesis which causes the formation of abnormal haemoglobin molecules. The resultant microcytic anaemia is the characteristic presenting symptom of thalassaemias.
Thalassaemia is a quantitative problem of globin synthesis, whereas sickle cell disease is a qualitative problem of synthesis of an incorrectly functioning globin.
Pathology
Normal adult haemoglobin is composed of HbA (98%) and HbA2 (2%). HbA contains two α globin chains and two β globin chains, and HbA2 contains two α globin chains and two δglobin chains. They are arranged into a heterotetramer. Patients with thalassaemia produce deficient α or β globin, unlike sickle cell disease patients, which produceswho produce a specific mutantabnormal form of β globin.
The thalassaemias are classified according to the affected chain of the haemoglobin molecule. In α thalassaemias, production of the α globin chain is reduced, while in β thalassaemia production of the β globin chain is reduced.
The β globin chains are encoded by a single gene on chromosome 11; α globin chains are encoded by two closely linked genes on chromosome 16. Thus, in a normal person with two copies of each chromosome, there are two loci encoding the β chain, and four loci encoding the α chain. Deletion of one of the α loci has a high prevalence in people of African or Asian descent, making them more likely to develop α thalassaemias. β thalassaemias are common in Africans, but also in Greeks and Italians.
The thalassaemia trait may confer a degree of protection against malaria, which confers a selective survival advantage on carriers.
Radiographic features
Skeletal
Ineffective haematopoiesis results in severe anaemia that in turn leads to an increase in erythropoietin. This increase results in an expansion of the bone marrow by a factor of up to 15 to 30 9. Conversion of yellow to red marrow occurs and in patients with uncontrolled disease marrow expansion results in an enlargement of the medullary space and thinning of cortical bone 8.
This expansion leads to the destruction of medullary trabeculae with initial cortical and trabecular thinning leading to a subsequent coarsening appearance that may lead to a "cob-webbing" pattern 9.
General features
osteoporosis and osteopenia 4,8
extramedullary haematopoiesis may appear as lobulated masses covering the anterior or posterior segments of the ribs on chest x-ray; extramedullary haematopoiesis is also more frequently seen in the posterior mediastinum compared to the anterior mediastinum or the pelvis 8
growth restriction 9
older patients tend to have signs of marrow proliferation in the axial skeleton with appendicular skeletal changes from early life regressing or completely disappearing 8
Skull
hair-on-end appearance (classic): unusual in patients after the age of nine in treated patients 8
thinning of the inner and outer table
the occipital bone is spared, due to a lack of hemopoietic bone marrow 6
Facial bones
rodent or chipmunk facies due to lateral displacement of the orbits (hypertelorism) with maxillary protrusion and ventral displacement of the incisors 8
hypopneumatisation of the frontal, maxillary, and sphenoid sinuses, filled with marrow containing bone 6
the ethmoid sinuses are spared due to lack of red bone marrow 6
dental malocclusion
Ribs
expansion of the ribs: especially at the costovertebral junctions 8
rib-within-a-rib appearance, noted particularly in the middle and anterior portions of the ribs 8,9
Spine
an initial increase in height to width ratio of vertebral bodies 9
gradual loss of height and biconcavity secondary to compression fractures 9
severe degree of medullary expansion can cause compression of the spinal cord in the thoracic region 8
scoliosis
Extremities
widening/expansion of the metacarpal and metatarsal shafts
premature fusion of the epiphyses 8,9
reduce longitudinal growth of long bones (humerus more than femur) 9
loss of concave shape in the long bones resulting in a convex shape 8
coarsening of the trabecular bone with cyst-like lucencies leading to a "worm-eaten" appearance 8
enlargement of nutrient foramina due to the activity of hyperplastic marrow 8,9
Gastrointestinal/hepatobiliary
Lungs
diffusion impairment
History and etymology
Thomas Benton Cooley (1871-1945) and Pearl Lee described a series of children with bone abnormalities and severe anaemia with associated splenomegaly in 1921 5. Thus the terms Cooley's anaemia or Cooley anaemia for thalessemia appear in some literature. ‘Thalassaemia’ was later coined in 1932 by George Hoyt Whipple (1878-1976), derived from the Greek word for "sea" (θάλασσα - thálassa) as the condition was identified in populations living near or originating from countries near the Mediterranean Sea 10.
-<p><strong>Thalassaemia</strong> is an autosomal recessive <a href="/articles/haemoglobinopathies">haemoglobinopathy</a> first described in the Mediterranean region. The genetic defect causes a reduction in the rate of globin chain synthesis which causes the formation of abnormal haemoglobin molecules. The resultant <a href="/articles/anaemia">microcytic anaemia</a> is the characteristic presenting symptom of thalassaemias.</p><p>Thalassaemia is a quantitative problem of globin synthesis, whereas <a href="/articles/sickle-cell-disease">sickle cell disease</a> is a qualitative problem of synthesis of an incorrectly functioning globin.</p><h4>Pathology</h4><p><a href="/articles/haemoglobin">Normal adult haemoglobin</a> is composed of HbA (98%) and HbA<sub>2</sub> (2%). HbA contains two <a href="/articles/a-globin-chains">α globin chains</a> and two <a href="/articles/b-globin-chains">β globin chains</a>, and HbA<sub>2</sub> contains two <a href="/articles/a-globin-chains">α globin chains</a> and two <a href="/articles/globin-chains">δ</a><a href="/articles/a-globin-chains"> </a><a href="/articles/globin-chains">globin chains</a>. They are arranged into a heterotetramer. Patients with thalassaemia produce deficient α or β globin, unlike sickle cell disease, which produces a specific mutant form of β globin.</p><p>The thalassaemias are classified according to the affected chain of the haemoglobin molecule. In α thalassaemias, production of the α globin chain is reduced, while in β thalassaemia production of the β globin chain is reduced.</p><p>The β globin chains are encoded by a single gene on chromosome 11; α globin chains are encoded by two closely linked genes on chromosome 16. Thus, in a normal person with two copies of each chromosome, there are two loci encoding the β chain, and four loci encoding the α chain. Deletion of one of the α loci has a high prevalence in people of African or Asian descent, making them more likely to develop α thalassaemias. β thalassaemias are common in Africans, but also in Greeks and Italians.</p><p>The <a href="/articles/thalassemia-trait">thalassaemia trait</a> may confer a degree of protection against malaria, which confers a selective survival advantage on carriers.</p><h4>Radiographic features</h4><h5>Skeletal</h5><p>Ineffective haematopoiesis results in severe anaemia that in turn leads to an increase in erythropoietin. This increase results in an expansion of the bone marrow by a factor of up to 15 to 30 <sup>9</sup>. Conversion of yellow to red marrow occurs and in patients with uncontrolled disease marrow expansion results in an enlargement of the medullary space and thinning of <a href="/articles/cortical-bone">cortical bone</a> <sup>8</sup>. </p><p>This expansion leads to the destruction of medullary trabeculae with initial cortical and trabecular thinning leading to a subsequent coarsening appearance that may lead to a "cob-webbing" pattern <sup>9</sup>. </p><h6>General features</h6><ul>- +<p><strong>Thalassaemia</strong> is an autosomal recessive <a href="/articles/haemoglobinopathies">haemoglobinopathy</a> first described in the Mediterranean region. The genetic defect causes a reduction in the rate of globin chain synthesis which causes the formation of abnormal haemoglobin molecules. The resultant <a href="/articles/anaemia">microcytic anaemia</a> is the characteristic presenting symptom of thalassaemias.</p><p>Thalassaemia is a quantitative problem of globin synthesis, whereas <a href="/articles/sickle-cell-disease">sickle cell disease</a> is a qualitative problem of synthesis of an incorrectly functioning globin.</p><h4>Pathology</h4><p><a href="/articles/haemoglobin">Normal adult haemoglobin</a> is composed of HbA (98%) and HbA<sub>2</sub> (2%). HbA contains two <a href="/articles/a-globin-chains">α globin chains</a> and two <a href="/articles/b-globin-chains">β globin chains</a>, and HbA<sub>2</sub> contains two <a href="/articles/a-globin-chains">α globin chains</a> and two <a href="/articles/globin-chains">δ</a><a href="/articles/a-globin-chains"> </a><a href="/articles/globin-chains">globin chains</a>. They are arranged into a heterotetramer. Patients with thalassaemia produce deficient α or β globin, unlike sickle cell disease patients, who produce a specific abnormal form of β globin.</p><p>The thalassaemias are classified according to the affected chain of the haemoglobin molecule. In α thalassaemias, production of the α globin chain is reduced, while in β thalassaemia production of the β globin chain is reduced.</p><p>The β globin chains are encoded by a single gene on chromosome 11; α globin chains are encoded by two closely linked genes on chromosome 16. Thus, in a normal person with two copies of each chromosome, there are two loci encoding the β chain, and four loci encoding the α chain. Deletion of one of the α loci has a high prevalence in people of African or Asian descent, making them more likely to develop α thalassaemias. β thalassaemias are common in Africans, but also in Greeks and Italians.</p><p>The <a href="/articles/thalassemia-trait">thalassaemia trait</a> may confer a degree of protection against malaria, which confers a selective survival advantage on carriers.</p><h4>Radiographic features</h4><h5>Skeletal</h5><p>Ineffective haematopoiesis results in severe anaemia that in turn leads to an increase in erythropoietin. This increase results in an expansion of the bone marrow by a factor of up to 15 to 30 <sup>9</sup>. Conversion of yellow to red marrow occurs and in patients with uncontrolled disease marrow expansion results in an enlargement of the medullary space and thinning of <a href="/articles/cortical-bone">cortical bone</a> <sup>8</sup>. </p><p>This expansion leads to the destruction of medullary trabeculae with initial cortical and trabecular thinning leading to a subsequent coarsening appearance that may lead to a "cob-webbing" pattern <sup>9</sup>. </p><h6>General features</h6><ul>
-</ul><h4>History and etymology</h4><p>Thomas Benton Cooley (1871-1945) and Pearl Lee described a series of children with bone abnormalities and severe anaemia with associated splenomegaly in 1921 <sup>5</sup>. ‘Thalassaemia’ was later coined in 1932 by George Hoyt Whipple (1878-1976), derived from the Greek word for "sea" (θάλασσα - thálassa) as the condition was identified in populations living near or originating from countries near the Mediterranean Sea <sup>10</sup>.</p>- +</ul><h4>History and etymology</h4><p>Thomas Benton Cooley (1871-1945) and Pearl Lee described a series of children with bone abnormalities and severe anaemia with associated splenomegaly in 1921 <sup>5</sup>. Thus the terms Cooley's anaemia or Cooley anaemia for thalessemia appear in some literature. ‘Thalassaemia’ was later coined in 1932 by George Hoyt Whipple (1878-1976), derived from the Greek word for "sea" (θάλασσα - thálassa) as the condition was identified in populations living near or originating from countries near the Mediterranean Sea <sup>10</sup>.</p>
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