CBC Basic Interpretation
CBC Basic Interpretation
Basic Interpretation
CBC
is one of the most common laboratory tests in medicine.
Typically, it includes the following:
White blood cell count (WBC or leukocyte count)
WBC differential count
Red blood cell count (RBC or erythrocyte count)
Hematocrit (Hct)
Hemoglobin (Hb)
Mean corpuscular volume (MCV)
Mean corpuscular hemoglobin (MCH)
Mean corpuscular hemoglobin concentration (MCHC)
Red cell distribution width (RDW)
Platelet count
Mean Platelet Volume (MPV)
ANEMIA
Microcytic
(MCV <80 fL)
Normocytic
(MCV 80-100 fL)
Macrocytic
(MCV >100 fL)
MICROCYTIC ANEMIA
The 3 major diagnostic possibilities for
microcytic amaenia are :
Iron deficiency anemia (IDA),
Thalassemia,
Anemia of chronic disease (ACD)
IDA
Thalassemia
Disproportionate !!!
Mentzer index
Is used to differentiate IDA from Bthalassemia.
MCV / RBC : is < 13, thalassemia is more
likely.
If the result > 14, then iron-deficiency
anemia is more likely.
ACD
Macrocytosis
Common causes:
Drug-induced
Nutritional
Liver disease, alcohol use
Hypothyroidism
Macrocytosis
RBC: normal
Hb: normal or low
MCV: high
RDW: normal or high
WBC
Leukopenia.
Leukocytosis.
Leucopenia
Common causes:
Chemotherapy
Radiation therapy
Leukemia (as malignant cells overwhelm the
bone marrow)
Myelofibrosis
Aplastic anema
Medications
Clozapine (anti-psychotic)
Immunosuppressive drugs
Interferons
Other causes :
Influenza
Systemic lupus erythematosus
Typhus
Malaria
HIV
Tuberculosis
Dengue
Rickettsial infections
Enlargement of the spleen
Folate deficiencies
Psittacosis
Sepsis
Pseudoleukopenia
It can develop upon the onset of infection.
The leukocytes are marginalized in the blood vessels so
that they can scan for the site of infection.
This means that even though there is increased WBC
production, it will appear as though it is low from a blood
sample, since the blood sample is of core blood and does
not include the marginalized leukocytes.
Valproic Acid
Leukocytosis
Neutrophil leucocytosis (neutrophilia >7.5x109/l):
Infection:
Inflammation /
necrosis:
Myeloproliferative
disorders:
Metabolic:
uraemia / acidosis
gout
eclampsia
Malignancy:
Drugs:
steroids
Blood loss:
Lymphocytosis:
Acute viral infection (usually associated with
rubella
pertussis
mumps
infectious mononucleosis
most other acute viral illnesses
hepatitis B and C
Bacterial infections:
tuberculosis
brucellosis
whooping cough
acute bacterial infections in infants
Other causes:
thyrotoxicosis
autoimmune disorders
lymphoma
lymphocytic leukaemias
neutropaenia):
Thrombocytopenia
Decreased production
Vitamin B12 or folic acid deficiency
Leukemia
Decreased production of thrombopoietin
Sepsis, systemic viral or bacterial infection
Hereditary syndromes
Congenital amegakyrotic thrombocytopenia
Thrombocytopenia absent radius syndrome
Fanconi anemia
Bernard-Soulier syndrome associated with large platelets
Meg-Hegglin anomaly
Grey platelet syndrome
Alport syndrome
Increased destruction
Thrombocytosis
Do not necessarily signal any clinical
problems, and are picked up on a routine
full blood count.
A full medical history must be elicited to
ensure that the increased platelet count is
not due to a secondary process.
Thrombopoetinan acute phase
reactant
Thrombocytosis
Essential (primary)
Essential thrombocytosis (a form of myeloproliferative
disease)
Other myeloproliferative disorders such as chronic
myelogenous leukemia, polycythemia vera,
myelofibrosis
Reactive (secondary)
Inflammation
Surgery (which leads to an inflammatory state)
Hyposplenism / spleenectomy
2.9
9.8
27
60
16.5
3.2
17.3
350