Indication of peripheral blood smear exmination: 1. For carried out differential WBC count. 2. For differential diagnosis of anemia. 3. For detection of parasites. 4. For diagnosis of leucemoid reaction. 5. For diagnosis and differential diagnosis of leukemia. 6. For detection of platelet abnormalities. 7. For diagnosis of conditions like infectious mononucleosis. 1) RBC series 2) WBC series 3) Platelets 4) Parasites 5) Other abnormal cells final diagnosis with advice
1. Abnormalities of Haemoglobin content:- Hypochromia Hyperchromia Anisochromia Polychromatophilia
2. Abnormalities of size of red cells:- Microcytosis Macrocytosis Anisocytosis 3. Abnormalities of shape of red cells ( Poikilocytosis ):- different abnormal shapes of RBC
I. Elliptocytosis II. Spherocytosis III. Target cells IV. Schistocytosis V. Acanthocytois VI. Crenated cells VII. Sickled cells VIII. Leptocytes 4. Abnormalities of structure of red cells:- •Basophilic stippling ( Punctate basophilia ) •Howell- jolly bodies •Cabot rings •Pappenheimer bodies •Malarial stippling •Rouleaux formation •Agglutination •Nucleated red cells •No nucleus, enzyme packets •Biconcave discs – Haem + Gl •Center 1/3 pallor •Pink cytoplasm (Hb filled) •Cell size 7- 8 µ - capill. 2 µ •EM pathway, HMP •Negative charge – no phago •Na less, K more inside •100-120 days life span
Hypochromic Microcytic
The RBC‘s here are smaller than normal and have an increased zone of central pallor. This is indicative of a hypochromic (less hemoglobin in each RBC) microcytic (smaller size of each RBC) anemia. There is also increased anisocytosis. Microcytic
the average size of erythrocytes is smaller than normal Macrocytic
Note the hypersegmented neurotrophil and also that the RBC are almost as large as the lymphocyte. Finally, note that there are fewer RBCs. Here. Elliptocytosis, Megaloblastic anaemia
ELLIPTOCYTE HS, AIHA, Thermal injury,Burns, Chemical poisoning, Hypophosphataemia
SPHEROCYTE Uraemia,Pyruvatekin ase defi.,Phosphoglycera te kinase defi.
ECHINOCYTES Disturbence in red cell cation composition Hereditary Stomatocytosis, Liver disease, Alcoholism
STOMATOCYTE Thalassemia Major, Microangiopathic Hemolytic anaemia, Cardiac Hemolytic anaemia Sickle cell anemia Thalassemia disorder, Sickle cell anaemia, Hb E & Hb C disease,Liver disease, after splenectomy
Terminology Description Condition
Target cells Central hemoglobin; target-shaped Liver disease; thalassemia: Abnormal Hgb; iron deficiency
Echinocyte Short spicules, equally-spaced Uremia, hypokalemia, artifact
Acanthocyte Spiculated, irregular Liver disease (alcohol), Post-splenectomy
Spherocyte Spherical, no central pallor HS, Immune hemolytic anemia Schistocyte Fragmented RBC, helmet cells MAHA, burns
Ovalocyte Oval/elliptical shaped Hereditary elliptocytosis, Megaloblastic anemia
Sickle cell bipolar spiculated shape Hgb S-containing “banana” shaped hemoglobinopathy
Teardrop cell single elongated extremity Myelophthistic changes
Bite cells Irregular gap in membrane G6PD deficiency Rouleaux formation Stacking of RBCs due to increased plasma proteins coating RBCs Agglutination Antibody-mediated clumping, temperature mediated Auto immune hemolytic anaemia
MICROCYTIC HYPOCHROMIC RBC
NORMOCYTIC NORMOCHROMIC RBC
G6PD Deficiency
Microcytic - Thalassaemia trait
Normocytic - Lead poisoning
Normo or micro - Sideroblastic anemia
Macrocytic - Megaloblastic anemia Post splenectomy Splenic atrophy Pernicious anaemia Coeliac disease RING OF P.VIVAX TROPHOZOITE OF P.VIVAX MULTIPLE RINGS OF P.FALCI GAMATOCYTE OF P.FALCI
Cells with 5 or more lobes are considered hypersegmented, e.g. megaloblastic changes Uraemia After cytotoxic drug treatment esp methotrexate
BLAST CELL BASOPHIL
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MYELOBLAST
MYELOCYTE Platelets are small, 1-3 µm in diameter, purple structures with tiny irregular projection on surface. Thrombocytopenia in malaria and dengue. Clumps of platelets Platelet satellitism.
Causes of false thrombocytopenia on automated heamatology analyzer: a)