Practical of Clinical Hematology

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Practical of Clinical Hematology. RBC’s Morphology. Lab 2. RBCs Abnormal morphology. Peripheral Blood Morphology. Abnormal erythrocyte morphology. Is found in pathological states that may be abnormalities in Red cell distribution. Size (anisocytosis). - PowerPoint PPT Presentation

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Practical of Clinical Hematology

Lab 2 RBC’s Morphology

RBCs Abnormal morphology

Peripheral Blood Morphology

Abnormal erythrocyte morphology Is found in pathological states that may be

abnormalities in I. Red cell distribution.II. Size (anisocytosis).III. Hemoglobin content – Color Variation .IV. Shape (poikilocytosis).V. The presence of inclusion bodies in

erythrocyte.

I. Erythrocyte Distribution Abnormalities Rouleaux formation

Stacking of RBCs due to increased plasma proteins coating RBCs (resembling a stack of coins)Found in:- Hyperfibrinogenaemia- Hyperglobulinaemia

AgglutinationAntibody-mediated Irregular clumping , temperature dependentFound in:- Cold agglutinins- Warm autoimmune hemolysis

II. Variation in erythrocyte size (anisocytosis)

Anisocytosis: Variations in size (Microcyte and Macrocyte)

Normocytic RBC’s Normal size of RBC (8 μm) with a range of 7 to 9 μm.

The nucleus of a small lymphocyte (± 8 µm) is a useful guide to the size of a red blood cell).

Microcytic RBC cell smaller than the normal RBC ( <7 μm), and is

associated with a decrease in hemoglobin synthesis Found in:

Iron deficiency anemia. Thalassaemia. Sideroblastic anemia. Lead poisoning. Anemia of chronic disease.

Macrocyte RBC larger than the normal (<9 μm) and is the result of a

defect in nuclear maturation or stimulated erythropoiesis. May be round or oval in shape, the diagnostic significance being different.

Found in: Folate and B12 deficiencies (oval) Ethanol (round) Liver disease (round) Reticulocytosis (round)

Example : Film Study

Most erythrocytes presented in the picture are microcytes (compare with the small lymphocyte). The degree of hemoglobinization is sufficient. Normal platelets and single ovalocytes are present.

1. microcyte   2. normocyte

III. Variation in erythrocyte color A normal erythrocyte has a pinkish-red color with a

slightly lighter-colored center (central pallor) when stained with a blood stain, such as Wright.

The color of the erythrocyte is representative of hemoglobin concentration in the cell.

Under normal conditions, when the color, central pallor, and hemoglobin are proportional, the erythrocyte is referred to as Normochromic.

Hypochromia Increased central pallor and decreased

hemoglobin concentration, the central pallor occupies more than the normal third of the red cell diameter. Found in:

Iron deficiency Thalassaemia any of the conditions

leading to Microcytosis

Polychromasia Red cells stain shades of blue-gray as a consequence of

uptake of both eosin (by hemoglobin) and basic dyes (by residual ribosomal RNA). Often slightly larger than normal red cells and round in shape - round macrocytosis.

Found in:Any situation with reticulocytosis – for example bleeding, hemolysis or response to heamatinic factor replacement

IV. Shape Abnormalities of Erythrocytes

Poikilocytosis is the general term for mature erythrocytes that have a shape other than the round, biconcave disk.

Poikilocytes can be seen in many shapes.(e.g. Acanthocyte, Spherocytosis,……)

Shape Abnormalities of ErythrocytesTerminology Description Condition

Target Cells Central Hemoglobin; target shaped

Liver Disease; Thalassaemia, Abnormal Hb; Iron Deficiency

Echinocyte Short specula's, equally-spaced

Uremia, Hypokalemia, Artifact

Acanthocyte Speculated, Irregular Liver disease (Alcohol), Post-spleenoctomy.

Spherocyte Spherical, no central pallor HS, immune Hemolytic anemiaShistocyte Fragmented RBC, Helmet

cellsMAHA, burns

Ovalocyte Oval / Elliptical shaped Hereditary elliptocytosis, Megaloblastic anemia.

Sickle Cell Bipolar speculated shape “ banana” shaped

Hb S-containing hemoglobinopathy

Teardrop cell Single elongated extremity

Myelophthistic changes

Bite cells Irregular gap in membrane G6PD deficiency

Red cell with a “target” or bull’s-eye appearance. The cell appears with a central bull’s eye that is surrounded by a clear ring and then an outer red ring.Found in:

Obstructive liver disease Severe iron deficiency Thalassaemia Haemoglobinopathies (S and C) Post splenectomy Lipid disorders

Target cell

Red cells are more spherical. Lack the central area of pallor on a stained blood film.Found in: Hereditary spherocytosis Immune haemolytic anemia Zieve's syndromeMicroangiopathic haemolytic

Spherocytosis:

Red cells with a central linear slit or stoma. Seen as mouth-shaped form in peripheral smear.Found in:- Alcohol excess- Alcoholic liver disease- Hereditary stomatocytosis

Stomatocytosis:

Ovalocyte :

An elongated oval cell. They are a result of a membrane defect.Found in: Thalassaemia major. Hereditary ovalocytosis. Sickle cell anemia

Elliptocytosis:The red cells are oval or elliptical in shape. Long axis is twice the short axis.

Found in:- Hereditary elliptocytosis- Megaloblastic anemia- Iron deficiency - Thalassaemia- Myelofibrosis

red cell fragments that are irregular in shape and size. They are usually half the size of the normal RBC; therefore, they have a deeper red color.

Found in: DIC Micro angiopathic haemolytic

anemia Mechanical haemolytic anemia

Schistocyte:

Have accentric hallow area. Resemble a women's handbag and may be called pocket-book cell.

Found in: Microangiopathic hemolytic anemia

Blister cell: pre keratocyte

Part of the cell fuses back leaving two or three horn-like projections. The keratocyte is a fragile cell and remains in circulation for only a few hours.

Found in:- Uraemia- Severe burns- EDTA artifact- Liver disease

Also called helmet cells

Keratocytes (horn cell)

Degmacyte "bite cell" An abnormally shaped red blood cell with one or more

semicircular portions removed from the cell margin. These "bites" result from the removal of denatured

hemoglobin by macrophages in the spleen. Found In:

G-6-PD deficiency, in which uncontrolled oxidative stress causes hemoglobin to denature and form Heinz bodies, is a common disorder that leads to the formation of bite cells

Sickle shaped red cells Found in: Hb-S disease and trait

Sickle Cells:

Red cell with 30 or more, short blunt projections which are regularly distributed on their surfaceFound in: Usually artifactual— the result of slow drying under humid conditions.Sometimes are non - artifactual, indicating uremia or pyruvate kinase deficiency. Hemolytic anemia Uremia. Megaloblastic anemia

Cells retain the central pallor.

Echinocyte “Burr” (crenation ) cell:

Echinocytes (Burr Cells)

Red blood cells with irregularly spaced projections, these projections very in width but usually contain a rounded end

Found in:- Liver disease - Post splenectomy- Anorexia nervosa and starvation

Acanthocytosis (Spur Cells):

Acanthocytes (Spur Cells)

Resembles a tear and usually smaller than the normal RBC.

Found in: Bone marrow fibrosis Megaloblastic anemia Iron deficiency Thalassaemia

Dacryocytes (Teardrop):

Envelope form cell

Found in Thalassaemia Sickle cell

anemia

V. Erythrocyte Inclusions with Wright’s Stain

Inclusion Composition

Appearance Condition

Basophilic stippling

Precipitated ribosomes

Evenly dispersed fine or coarse granules

- Lead poisoning- Thalassaemia ,

other anemia.

Howell-Jolly bodies

DNA in originNuclear Fragment

Dense, round blue granule

Post – Splenectomy

Pappenheimer bodies

Iron-containing granules

Small blue granules in clusters

Anemia's

Heinz bodies Denatured Hemoglobin

Round blue precipitates

G6PD

Cabot Rings Remnants of Nuclear membrane

Reddish-blue thread like rings

Severe anemia, Lead poisoning.

Organism Small blue inclusion

MalariaBabesiosis

Small round cytoplasmic red cell inclusion with same staining characteristics as nuclei

Found in: Post splenectomy Megaloblastic anemia

Howell-Jolly Bodies:

These are iron containing granules in red blood cells that are seen because the iron is aggregated with mitochondria and ribosomes. They appear as faint violet or magenta specks, often in small clusters, due to staining of the associated protein. They are associated with severe anemias and thalassemias. Pappenheimer bodies can be increased in hemolytic anemia, infections and post-splenectomy.

Siderotic Granules (Pappenheimer Bodies)

Considerable numbers of small basophilic inclusions in red cells. Found in:- Thalassaemia- Megaloblastic anemia- Hemolytic anemia - Liver disease- Heavy metal poisoning.

Basophilic stippling:

Represent denatured hemoglobin (methemoglobin - Fe+++) within a cell. With a supravital stain like crystal violet, Heinz bodies appear as round blue precipitates. Presence of Heinz bodies indicates red cell injury and is usually associated with G6PD-deficiency.

Heinz Bodies:

Heinz Body Preparation. RBC are incubated supravitally in new Methylene blue to identify precipitates of oxidatively denatured hemoglobin.

Reddish-blue threadlike rings in RBCs of severe anemia's. These are remnants of the nuclear membrane or remnants of microtubules and appear as a ring or figure 8 pattern. Very rare finding in patients with 1. Megaloblastic anemia. 2. severe anemia's.3. lead poisoning.4. Dyserythropoiesis.

Cabot Rings:

A - Cabot ringB - Howell-Jolly body

Two organisms are have a tendency to invade the RBCs.1. All 4 species of the malaria parasite will invade RBCs. We

will see the Plasmodium of different species in RBCs.2. Theileria microti (Bebesia microti)

Parasites of Red Cell:

Malaria

RBCs Abnormal morphologyDepiction of red blood cell morphologies that may appear on a peripheral smear, showing: (A) basophilic stippling, (B) Howell-Jolly bodies, (C) Cabot's ring bodies and (D) Heinz's bodies.

Blood Film in Some Cases

Normal Peripheral Smear

Autoimmune Hemolytic Anemia

Spherocytes

Hereditary Spherocytosis

Spherocytes

Hereditary pyropoikilocytosis

Microangiopathic Hemolytic Anemia

Schistocytes

Sickle Cell Anemia

Hb SS

Idiopathic myelofibrosis

Dacryocytes

Iron Deficiency Anemia

Severe Hypochromia

Treated Iron Deficiency Anemia

Mixed Population:

Alpha Thalassaemia (a-/--)

Microcytic Hypochromia

Target Cells Spur Cells

Morphologic Changes in Liver Disease

Hepatorenal Syndrome

Burr + Spur Cells