Complete Blood Count (CBC)
Main parameters measured
1. Hb concentration.
2. ESR
3. Haematocrit (Hct) or PCV.
4. White cell count.
5. WBC differential.
6. Red cel count (RCc)
7. MCV
8. MCH
9. MCHC
10. Red cell distribution width (RDW).
11. Platelet count.
Hemoglobin
• Interpretation
Increased Hb:
(18.5 in Male & 16.5 in Female)
• PRV (Polycythaemia Rubra Vera)
Decreased Hb:
• Anaemia
Spurious low Hb:
• Improper sample mixing
• Blood taken from vein into which an
infusion is flowing
Erythrocyte sedimentation rate (ESR)
• Interpretation
Increased ESR
1. Acute bacterial, fungal or viral
infection
2. Necrotising bacterial infection
3. Acute inflammatory diseases, e.g.
Crohn's disease, polymyalgia
rheumatic
4. Chronic bacterial or fungal infection,
e.g. localized abscess, bacterial
endocarditis or tuberculosis
5. SLE, Sjögren's syndrome
6. Multiple myeloma
7. Pregnancy, old age, end-stage renal
disease
Decreased ESR
1. Polycythaemia
2. Hypofibrinogenaemia
3. CCF
4. Poikilocytosis
5. Spherocytosis
6. Sickled cells
Hematocrit (HCT)
• Interpretation
Increased HCT
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
Decreased HCT
Anaemia
Red cell count (RCC)
• Interpretation
Decreased Red cell count
1. Hypoproliferative anaemias, e.giron,
vitamin B12 and folate deficiencies.
2. Aplasias e.g. idiopathic or drug-
induced (don't forget chemotherapy).
3. Parvovirus B19 infection-induced red
cell aplasia resulting in transient
marked anaemia.
Increased Red cell count
1. PRV
2. Thalassaemia.
Total White Cell Count
• Interpretation
Increased WBCS (Leucocytosis)
• Infection (esp. Bacterial)
• Leukaemia
• Myocardial Infarction
Decreased WBCS (Leucopenia)
• Infection (eg. Typhoid,Viral, Protozoal)
• Pancytopenia due to any cause
Differential White Cell Count
• Interpretation
Increased Neutrophils (Neutrophilia)
• Infection: bacterial, fungal
• Trauma: Surgery, burns
• Infarction: myocardial infarct,
pulmonary embolus, sickle-cell crisis
• Inflammation: gout, rheumatoid
arthritis, ulcerative colitis, Crohn's
disease
• Malignancy: solid tumours, Hodgkin
lymphoma
• Myeloproliferative disease:
polycythaemia, chronic myeloid
leukaemia
• Physiological: exercise, pregnancy
Decreased Neutrophils (neutropenia)
• Infection: viral, bacterial (e.g.
Salmonella), protozoal (e.g. malaria)
• Drugs: Carbimazole, propylthiouracil,
captopril, nifedipine, pyrimethamine,
sulfadoxine, chloroquine,
sulphonamides, penicillins,
cephalosporins
Autoimmune: connective tissue
disease
• Alcohol
• Bone marrow infiltration: leukaemia,
myelodysplasia
• Congenital: Kostmann's syndrome
• Constitutional: Afro-Caribbean and
Middle Eastern descent
Increased Eosinophils: (eosinophilia)
• Allergy: hay fever, asthma, eczema
• Infection: parasitic
• Drug hypersensitivity: e.g. gold,
sulphonamides
• Vasculitis-
• Churg-Strauss syndrome
• Granulomatosis with polyangitis
(Wegener's granulomatosis)
• Polyarteritis nodosa
• Malignancy: solid tumours,
Iymphomas
• Primary bone marrow disorders:
• Myeloproliferative disorders,
• Hypereosinophilic syndrome (HES)
• Acute myeloid leukaemia
Increased Basophils (Basophilia)
• Myeloproliferative disease:
polycythaemia, chronic myeloid
leukaemia
• Inflammation: acute hypersensitivity,
ulcerative colitis, Crohn's disease
• Iron deficiency
Increased Monocytes (Monocytosis)
• Infection: bacterial (e.g. tuberculosis)
• Inflammation: connective tissue
disease, ulcerative colitis, Crohn's
disease
• Malignancy: solid tumours, chronic
myelomonocytic leukaemia
Increased Lymphocytes (Lymphocytosis)
• Infection: viral, bacterial (e.g.
Bordetela pertussis)
• Lymphoproliferative disease: chronic
lymphocytic leukaemia, lymphoma
• Post-splenectomy
Decreased Lymphocytes (Lymphopenia)
• Inflammation: connective tissue
disease
• Lymphoma
• Renal failure
• Sarcoidosis
• Drugs: corticosteroids, cytotoxics
• Congenital: severe combined
immunodeficiency
• HIV infection
Platelet count
Interpretation
Decreased Platelet count(Thrombocytopenia)
Marrow hypoplasia
• Childhood bone marrow failure
syndromes, e.g. Fancon's anaemia,
dyskeratosis congenita,
amegakaryocytic thrombocytopenia
• Idiopathic aplastic anaemia
• Drug-induced: cytotoxics,
antimetabolites
• Transfusion-associated graft-versus-
host disease
Marrow infiltration
• Leukaemia
• Myeloma
• Carcinoma (rare)
• Myelofibrosis
• Osteopetrosis
• Lysosomal storage disorders, e.g.
Gaucher's disease
Haematinic deficiency
• Vitamin B12 and/or folate deficiency
Familial (macro-) thrombocytopathies
• Myosin neavy chain abnormalities, e.g.
Alport's syndrome, Fechner's
syndrome
• Bernard Soulier disease
• Montreal platelet syndrome
• Wiskott-Aldrich syndrome (small
platelets)
Immune mechanisms
• Idiopathic thrombocytopenic purpura*
• Neonatal alloimmune
thrombocytopenia
• Post-transfusion purpura
• Drug-associated, especially quinine
and vancomycin
Coagulation activation
• Disseminated intravascular
coagulation
Mechanical pooling
• Hypersplenism
Thrombotic microangiopathies
• Haemolytic uraemic syndrome
Liver disease
• Thrombotic thrombocytopenic purpura
Pre-eclampsia
Infection with Thrombocytopenia
• Malaria, kala-azar
VHF including Dengue, Yellow fever,
Ebola fever
• Meningococcaemia
• Enteroviruses
• Leptospirosis
• Rubella
• Epstein-Barr virus, Cytomegalovirus,
HIV
• Louse-borne relapsing fever
• Primary toxoplasmosis and secondary
syphilis.
Others
• Gestational thrombocytopenia
• Type 2B von Willebrand disease
Note: Spuriously low due to clot in
sample, platelet clumping.
Increased Platelet count (Thrombocytosis)
Reactive thrombocytosis
• Chronic inflammatory disorders
• Malignant disease
• Tissue damage
Haemolytic anaemias
• Post-splenectomy
• Post-haemorrhage
Clonal thrombocytosis
• Primary thrombocythaemia
PRV
• Chronic myeloid leukaemia
• Myelofibrosis
• Myelodysplastic syndromes (RARS
with thrombocytosis, 5 q- syndrome)
1 Comments
It's complete package
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