Erythrocye Pathologies Flashcards

(21 cards)

1
Q

What is anaemia and what are the signs and symptoms?

A

A deficiency in haemoglobin.

S&S: fatigue, tachycardia, pallor, palpitations

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2
Q

What is iron-deficiency anaemia and the causes

A

Reduced concentration of haemoglobin in erythrocytes causing them to appear paler. Hypochromic microcytic anaemia

Causes:
Deficient dietary intake
Malabsorption 
Excessive blood loss
Excess requirements (pregnancy/rapid child growth)
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3
Q

What are the signs of iron deficiency anaemia?

A

Koilynchia, angular stomatitis, glossitis, brittle hair, tachycardia

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4
Q

Define megaloblastic Anaemia

A

Characterised by large, immature and dysfunctional red blood cells

Folic acid & B12 are required for DNA synthesis

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5
Q

What are the causes of megaloblastic anaemia?

A

✅Deficient dietary intake of folic acid & folate
✅lack of intrinsic factor
✅malabsorption
✅drugs

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6
Q

What is hypo/aplastic anaemia and what are the causes, signs, symptoms and treatment?

A

Failure of haemopoiesis
Pancytopenia - absence of all three cells

Causes: idiopathic, congenital, secondary to drugs

S&S:
anaemia (pallor, headache, dyspnoea, palpitations.
Multiple infections
Easy bleeding

Treatment: bone marrow stem cell transplant, platelet/blood transfusion

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7
Q

What is haemolytic anaemia?

A

Excessive breakdown of RBCs. RBC life span 5 days

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8
Q

What is sickle cell anaemia and how is it caused?

A

Deficiency of the 2 alpha/2 beta formation of haemoglobin (HbS) and causes it to sickle up.

When HbS gives up oxygen to interstitial fluid it caused the erythrocyte to sickle up (crescent shape)

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9
Q

What causes sickle cell anaemia and its signs and symptoms?

A

✅Inherited recessive condition (substitution chromosome 21)
✅Afro-Caribbean
✅protect against malaria

S&S:
Usually begins 3-6 months
Same signs as anaemia
Splenomegaly and jaundice

Blood tests FBC and blood film.

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10
Q

What is thalassaemia and its signs and symptoms?

A

Thalassaemia is associated with a defect in synthesis of either the alpha or beta haemoglobin chain.

An inherited disease

S&S:
B-thalassaemia = starts when HbA production begins
A-thalassaemia = can be lethal in utero.

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11
Q

What is polycythaemia and its causes and signs and symptoms?

Clue: EPO on acid!

A

Excess production of erythrocytes resulting in increased blood viscosity, reduced blood flow and fish of thrombosis.

Causes:
physiological - high altitude
Pathological: unknown/genetic

Signs and symptoms;
arterial thrombosis: MI, pulmonary embolism, stroke
Venous thrombosis: DVT
Hypertension, pruritus, red skin, headaches, dizziness

Treat underlying cause. Prevent blood clots.

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12
Q

What is leukocytosis and causes?

A

Increase in the number of leukocytes.

Causes: leukaemia, response to infection

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13
Q

What is leukaemia?

A

Leukaemia is cancers of the bone marrow, characterised by an abnormal over production of leukocytes.

Results in suppressed production of erythrocytes and thrombocytes.

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14
Q

Describe and compare acute and chronic leukaemia?

A

Acute leukaemia: rapid onset, aggressive, immature cells

Chronic leukaemia: insidious onset. More differentiated cells.

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15
Q
Acute leukaemia
Age: all ages
Onset: sudden
Leukaemic cells: immature (-blasts)
Anaemia: prominent
Thrombocytopenia: prominent
Leukocyte count: variable
Lymph node enlargement: mild
Splenomegaly: mild
A
Chronic leukaemias:
Age: usually adults
Onset: insidious
Leukaemic cells: mature
Anaemia: mild
Thrombocytopenia: mild
Leukocyte count: increased
Lymph node enlargement: prominent
Splenomegaly: prominent
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16
Q

What are the 4 types of leukaemia?

What are the key signs and symptoms?

A
  1. Acute myelogenous leukaemia (AML)
  2. Acute lymphocytic leukaemia (ALL)
  3. Chronic myeloid leukaemia (CML)
    Chronic lymphocytic leukaemia (CLL)

S&S: malaise, anaemia (fatigue, pallor etc), frequent infections, easy bleeding/bruising

splenomegaly, enlarged lymph node, fever, weight loss

17
Q

How would you diagnose and treat leukaemia?

A

FBC: anaemia, low thrombocytes, variable leukocyte count
Blood film
Bone marrow transplant

Allopathic treatment: chemotherapy, bone marrow transplant, radiotherapy, immunotherapy.

18
Q

What is thrombocytopenia its signs and symptoms and causes?

A

Reduction in thrombocyte count

S&S: excessive bleeding, bruising, petechiae (small bleeding under skin)
Haematuria (blood in urine) haematemesis, (blood in vomit) bleeding gums PPH

Causes: leukaemia, congenital (from birth), radiation, drugs, chemo

19
Q

Describe haemophilia? What are the two types?

A

A deficiency in clotting factors.

Haemophilia A: deficiency of clotting factor 8

Haemophilia B: deficiency of clotting factor 9

Cause: genetic. X linked recessive disorder. Usually affects 1 in 5000 males. Females normally carriers.

20
Q

Haemophilia

When the mother carries the haemophilia gene and the father is unaffected

There is 50% chance that a son will have haemophilia. There is a 50% chance that a daughter will be a carrier

A

Haemophilia

When the father has haemophilia and the mother is unaffected

None of the sons will have haemophilia. All of the daughters will carry the haemophilia gene.

21
Q

What is Von Wilebrand disease? (vWD)

What causes it and what are the signs and symptoms?

A

A blood coagulation disorder, resulting from deficiency or abnormal function of a coagulation factor.

Usually asymptomagic, detected in woman with heavy menses.

Cause: genetic