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COMMON

DISORDERS OF
BLOOD CELLS

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Functions of blood
 Supply of oxygen to tissues (bound to
haemoglobin which is carried in red cells)
bound to plasma proteins (e.g. blood lipids)
 Removal of waste such as carbon dioxide,
urea and lactic acid
 Immunological functions, including circulation
of white cells, and detection of foreign
material by antibodies

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 Coagulation, which is one part of the body's
self-repair mechanism
 Messenger functions, including the transport
of hormones and the signalling of tissue
damage
 Regulation of body pH (the normal pH of
blood is in the range of 7.35 - 7.45)
 Regulation of core body temperature

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ANAEMIA
 Anaemia is a deficiency of red blood cells, or
insufficient haemoglobin within the red blood
cells.
 Usually this is because there are low levels of
haemoglobin in the blood or due to production
of faulty haemoglobin

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TYPES OF ANAEMIAS

IRON DEFICIENCY ANAEMIA


 It is caused by a lack of dietary iron, and there
is not enough of this mineral to form sufficient
haemoglobin.

 A person with this type of anaemia may have a


normal RBC count and a normal haematocrit,
but the haemoglobin level will be below
normal.

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PERNICIUOS ANAEMIA
 A deficiency of vitamin B12, which is found
only in animal foods, leads to pernicious
anaemia, in which the RBCs are large,
misshapen, and fragile.
 Another cause of this form of anaemia is lack
of the intrinsic factor due to autoimmune
destruction of the parietal cells of the
stomach lining.

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MEGALOBLASTIC ANAEMIA
 This is due to deficiency of folic acid
 It may be due to dietary deficiency e.g. in
infants if there is delay in establishing a mixed
diet, in alcoholism, in anorexia and in
pregnancy
 Also due to malabsorption from jejunum
caused by coeliac disease, tropical sprue
 Interference with folate metabolism by eg,
cytotoxic and anticonvulsant drugs
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SICKLE CELL ANAEMIA
 It is a genetic disorder of haemoglobin (Hb-
S), which causes RBCs to sickle, clog
capillaries, and rupture.
 Even though erythropoiesis is stimulated by
the loss of the cells, it cannot keep pace with
haemolysis.
 Acute episodes (sickle crises) caused by
blockade of small vessels cause acute pain in
the affected area often the hands and feets

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APLASTIC ANAEMIA
 It is suppression of the red bone marrow,
with decreased production of RBCs, WBCs,
and platelets.
 This is a very serious disorder that may be
caused by exposure to radiation, certain
chemicals such as benzene, or some
medications.

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THALASSAEMIA
 It is an inherited condition commonest in
Meditteranean countries
 It is caused by abnormal haemoglobin
production which in turn reduces
erythropoiesis and stimulates hemolysis
 The resultant anaemia may present in a
range of forms from mild and
asymptomatic to profound and life
threatening

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HAEMOLYTIC ANAEMIA
 It is any disorder that causes rupture of RBCs
before the end of their normal life span.
 Sickle-cell anaemia, thalassaemia and Rh
disease of the new-born are examples.
 Another example is malaria, in which a
protozoan parasite reproduces in RBCs and
destroys them.
 Haemolytic anaemias are often characterized
by jaundice because of the increased
production of bilirubin.

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HAEMOPHILIA
 Haemophilia is an inherited deficiency of
clotting in which bleeding may occur
spontaneously or after only minor trauma.
 Different types of haemophilia are due to
deficiencies of different blood clotting
factors and exhibit varying degrees of
severity, ranging from mild to severe
bleeding tendencies

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LEUKEMIA
 The term leukaemia refers to a group of red bone
marrow cancers in which abnormal white blood cells
multiply uncontrollably
 The accumulation of the cancerous white blood cells
in red bone marrow interferes with the production of
red blood cells, white blood cells, and platelets
 As a result the oxygen-carrying capacity of the blood
is reduced, an individual is more susceptible to
infection, and blood clotting is abnormal
 The cause of most types of leukaemia is unknown

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VITAMIN K DEFICIENCY
 Vitamin K is not involved in actual clot formation
but it is required for the synthesis of four clotting
factors.
 It is a fat-soluble vitamin that can be absorbed
through the lining of the intestine and into the
blood if absorption of lipids is normal
 People suffering from disorders that slow
absorption of lipids (for example, inadequate
release of bile into the small intestine) often
experience uncontrolled bleeding as a
consequence of vitamin K deficiency
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ROLE OF VITAMIN K IN
BLOOD CLOTTING
 Normal clotting depends on adequate levels of
vitamin K in the body
 Although vitamin K is not involved in actual
clot formation, it is required for the synthesis
of four clotting factors
 Normally produced by bacteria that inhabit the
large intestine

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 vitamin K is a fat-soluble vitamin that can be
absorbed through the lining of the intestine and
into the blood if absorption of lipids is normal
 People suffering from disorders that slow
absorption of lipids (for example, inadequate
release of bile into the small intestine) often
experience uncontrolled bleeding as a
consequence of vitamin K deficiency

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THROMBOSIS
 It is the formation of a clot in the blood that either
blocks, or partially blocks a blood vessel.
 The thrombus may lead to infarction, or death of
tissue, due to a blocked blood supply.
 The pathologic form of haemostasis is thrombosis.
It involves blood clot (thrombus) formation in
uninjured vessels or thrombotic occlusion of a
vessel after relatively minor injury.

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Both hemostasis and thrombosis involve three
components, the vascular wall, platelets, and
the coagulation cascade.
Factors.
 Age (as the age increases so the risk)
 Obesity

 Varicose veins

 Immobility

 Pregnancy

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 High estrogen levels

 Previous history of DVT

 Surgery and trauma of the pelvis, lower limbs

 Heart failure

 Recent myocardial infarction

 Lower limb paralysis

 Cigarette smoking

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EMBOLISM
 An embolism is an obstruction in a blood
vessel due to a blood clot or other foreign
matter that gets stuck while travelling through
the bloodstream.
 Emboli have moved from the place where they
were formed through the bloodstream to
another part of the body, where they obstruct
an artery and block the flow of blood.

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 The emboli are usually formed from blood
clots but are occasionally comprised of air, fat,
or tumour tissue.
 Embolic events can be multiple and small, or
single and massive.
 They can be life-threatening and require
immediate emergency medical care

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VON WILLEBRAND DISEASE
 This is the most common inherited bleeding
disorder occurring as frequently as 1 in 1000
individuals
 Von willebrand factor helps platelets adhere to
collagen and become activated.
 In this disease, platelet plug formation and the
contribution of activated platelets to blood
clotting are impaired.

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