hgd ال بسم الله الرحمن الرحیم In the name of ALLAH
DIAGRAMATIC REPRESENTATION OF BONE MARROW PLURIPOTENT
PCV or Hematocrit 57% Plasma 1% Buffy coat – WBC 42% RBCs Blood components
Interpretation of CBC- complete blood count
Results of lab.tests May be affected by Activity Diet Stress Geography medications Time of the day
Component of the CBC White Blood Cells ( WBC s) Red Blood Cells ( RBC s) Hemoglobin ( Hgb ) Hematocrit ( Hct ) Mean Corpuscular Volume ( MCV ) mean corpuscular hemoglobin( MCH ) Mean Corpuscular Hemoglobin Concentration ( MCHC ) Red cell distribution width ( RDW ) Platelet ( PLT )
RBC RBC (varies with altitude): M : 4.7 to 6.1 x10^12 /L F : 4.2 to 5.4 x10^12 /L In : 4.8 to 7.1 x10^12 /L Function : - transport hemoglobin which carries oxygen from the lung to the tissues -acid –base buffer.
( Hgb / Hb ) M: 14 to 18 g/ dL F : 12 to 16 g/ dL In: 14 to 24 g/dl 5> Hgb >20 Emergency Hemoglobin
Hematocrit (HCT /PCV) It is ratio of the volume of red cell to the volume of whole blood. M: 42 to 52 % F : 37 to 47 % In: 44 to 64 % 15> Hct >60 Emergency
MCV = mean corpuscular volume HCT/RBC count = 80-100fL small = microcytic normal = normocytic large = macrocytic MCHC = mean corpuscular hemoglobin concentration HB/RBC count = 26-34% decreased = hypochromic normal = normochromic MCV&MCHC
MCH (mean corpuscular hemoglobin) HB/HCT = 27-32 pg RDW (red cell distribution width) It is correlates with the degree of anisocytosis _ Normal range from 10-15% MCH & RDW
The causes of a hypochromic microcytic anaemia . These include lack of iron (iron deficiency), or of iron release from macrophages to serum ( anaemia of chronic inflammation or malignancy). Failure of protoporphyrin synthesis ( sideroblastic anaemia ) or of globin synthesis (Alpha or Beta Thalassaemia ).
RDW Megaloblastic anemias IDA Hemoglobinopathies Hemolotic anemia
Microcytic Hypochromic - IDA
Macrocytosis -MBA
Norms of leukocytes(WBC) A :4-11000/mm3 In:9-30000/mm3 30000<WBC<2500 Emergency
WBC The type of cell affected depends upon its primary function: In bacterial infections , neutrophils are most commonly affected In viral infections, lymphocytes are most commonly affected In parasitic infections, eosinophils are most commonly affected.
Abnormal result of WBC Leukocytosis _ Infectious diseases _Inflammatory disease(such as RA &allergy) _Leukemia _Severe emotional or physical stress _Tissue damage (e.g. necrosis,or burns)
Leukopenia : Decreased WBC production from BM Irradiation Exposure to chemical or drugs Autoimmune disease Acute infection
Function: Phagocytosis of bacteria and cell debris Neutrophil
Neutrophilia Conditions associated with : 1-Bacterial infections (most common cause) 2-Tissue destruction e.g. tissue infarctions, burns. 3- leukemoid reaction 4-Leukemia
Neutropenia – this may result from: 1-Decreased bone marrow production e.g. BM hypoplasia . 2-Ineffective bone marrow production E.g. megaloblastic anemias and myelodysplastic syndromes. 3- post acute infection _ e.g. typhoid fever, brucellosis.
Eosinophil Function: Involved in allergy , parasitic infections
Eosinophilia may be found in Parasitic infections Allergic conditions and hypersensitivity reaction
Basophilia . Most uncommon Seen in systemic hypersensitivity.
T cells: cellular ( for viral infections) B cells: humoral (antibody) Natural Killer Cells Lymphocyte
Lymphocytosis _ Viral infection e.g. Infectious mononucleosis, CMV or pertussis . _ Bacterial infection e.g. TB Lymphopenia _Stress _Steroid therapy _ Irradiation & immunodeficincy disease
Platelets Nor mal range; 150-400x10^3 /mm3 Destroyed by macrophage cells in the spleen . Function; involved in coagulation and blood haemostasis . 50000 >PLT>1x10^6 Emergency
Thrombocytosis Exercise . High attitudes. Splenectomy RA Thrombocytopenia Hypersplenism Haemorrhage. Bone marrow destruction or suppression e.g. Leukemia DIC Anemia Platelets
Petechial hemorhage . Easy bruising. Mucosal bleeding e.g. _ epistaxes . _ gum bleeding Manifestation of thrombocytopenia
PANCYTOPENIA 1. Aplastic Anaemia 2. Megloblastic Anaemia Bone marrow infiltration by leukaemias , lymphomas, multiple myeloma etc. 4. Myelofibrosis 5. Hypersplenism ( peripheral blood pancytopenia with normocellular or hypercellular marrow and splenomegaly )