Red Blood Cell

Protocols

HYPOCHROMIA (Increase in central pallor)
Iron deficiency anaemia
Thalassaemia
Sideroblastic anaemia
Anaemias of chronic diseases


MACROCYTES
(Larger than small lymphocytes)
Myeloblastic anaemia
Hepatic disease
B deficiency
Aplastic anaemia
Congenital dyserythropoietic anaemia
Pure red cell aplasia


TARGET CELLS
Obstructive liver disease
Thalassaemia
Haemoglobin ‘C’ disease
Haemoglobin ‘D’ disease


SPHEROCYTES
Hereditary spherocytes
Autoimmune haemolytic anaemia
Cl. welchii infection
Post-burn patients


LEUCOERYTHROBLASTIC PICTURE
(Immature myeloid and erythroid cells
appearing in peripheral blood)
Myeloproliferative disorders:
Polycythemia vera
Myelofibrosis
Haemolytic anaemias
Leukaemias
Bone marrow involvement with Hodgkin’s
carcinoma or lymphoma
Leukaemoid reactions.


RETICULOCYTE COUNT
Stained with brilliant cresyl blue appears as bluish
strands in cytoplasm due to precipitation of ribosomes
and RNA.
(Normal 0.1-2%).
Increased
Haemolytic anaemia
Nutritional anaemia on therapy

Reduced:

 -Aplastic anaemia
PNH.


INCREASED PLASMA HAEMOGLOBIN

(Normal 0.4 mg/100 ml)
G6 PD deficiency
PNH
Black water fever
Cold haemoglobinuria
Autoimmune haemolytic anaemia.


LEUCOCYTE ALKALINE
PHOSPHATASE SCORE

Increased
Infection
Leukaemoid reaction
Myelofibrosis
Aplastic anaemia
Polycythemia vera.
Decreased
Chronic myeloid leukaemia
Paroxysmal nocturnal haemoglobinuria.



COOMB’S TEST
It is positive in autoimmune haemolytic anaemia
i. Idiopathic.


ii. Secondary to
Lymphoma
Infectious mononucleosis
Mycoplasma pneumonia
Cold agglutinin disease

ESR raised
Pregnancy from 4th month
Anaemia (except sickle cell)
Acute myocardial infarction
Carcinomatosis
Pulmonary tuberculosis
Acute gout
Extensive tissue damage-burns
Acute infections
After fracture and operation.

ESR very rapid increase
 Temporal arteritis
 Kala-azar
 Some cases of multiple myeloma
 Rheumatoid arthritis
 Leukaemia
 Haemolytic anaemia
 Chronic renal disease
 Sarcoidosis

ESR decreased
Polycythaemia vera
Congestive cardiac failure
Whooping cough, dehydration.


COAGULATION TIME
Normal values for clotting time are 9-15 minutes.
Reduced
After meals
In typhoid
After haemorrhage and general anaesthesia
In endocarditis
After splenectomy.
Prolonged
In haemophilia A, B, and Factor XI deficiency
Obstructive jaundice
Chloroform and phosphorus poisoning. Here the
fibrinogen forming function of liver in hampered
Excessive CO2 in blood
Occasionally in leukaemia.

 

HCT: increase

1. Plasma Leakage (eg. In Dengue)

2. Polycythaemia Rubra Vera (>0.52

males, > 0.48 females)

3. True' polycythaemia (-Absolute

erythrocytosis)

Males > 0.60

Females > 0.56

4. Relative erythrocytosis

Diuretics

Smoking

Obesity

Alcohol excess

Gaisbock's syndrome

 

 

HCT: decrease

Anaemia

↑MCHC: Increase

1. Severe prolonged dehydration.

2. Hereditary spherocytosis.

3. Cold agglutinin disease.

 


MCHC: decrease

1. Iron deficiency anaemia.

2. Thalassaemia.

MCV (Macrocytosis):

1. B12 or folate deficiency

2. Myelodysplasia

Note: Spuriously raised in cold

agglutinins, non-ketotic hyperosmolarity

MCV (Microcytosis)

1. Iron deficiency

2. Thalassaemia traít

3. Sideroblastic anaemia

MCV normal (in anaemia)

1. Blood loss

2. Anaemia of chronic disease