peripheral smear..rbc disorders.. dr.padmesh

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Page 1: Peripheral smear..RBC disorders.. Dr.Padmesh

Dr.Padmesh. V

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Acanthocytes are seen in:

• Hereditary abetalipoproteinemia• Hereditary acanthocytosis• End stage liver disease• Anorexia nervosa• Malnutrition• Post splenectomy• Intravenous hyperalimentation particularly with intralipid infusion

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Bite cells are red cells from which precipitated denaturedhemoglobin has been removed by the spleen. The “bite” appears as half a circle removed from the edge of the red blood cell.

Bite cells are commonly seen in:

• Glucose 6 phosphate dehydrogenase (G-6-PD) deficiency• Unstable hemoglobin variants• Congenital Heinz body anemia (congenital bite cell anemia)

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Echinocytes are commonly seen in:

• Artifact due to slow drying of the smear because of high humidity• Renal disease• Liver disease• Pyruvate kinase deficiency

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Fragmented red cells are red cells that are injured and torn due to a microangiopathic process in which fibrin strands are generated and are responsible for injury to the red cells.

Fragmented cells are commonly seen in:

• Hemolytic uremic syndrome (HUS)• Thrombotic thrombocytopenic purpura (TTP)• Disseminated intravascular coagulation (DIC)• Other microangiopathic hemolytic anemias

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Sickle cells are red cells with two pointed ends which are in the shape of a crescent or sickle. This is due to the polymerization of deoxygenated hemoglobin S causing changes to the red blood cell making it less deformableand much more rigid.

Sickle cells are usually seen in:

• Sickle cell anemia• Hemoglobin SC• S beta thalassemia• Hemoglobin SD

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Target cells have a central hemoglobinized area within the surrounding area of pallor.

Target cells are commonly seen in:

• Hemoglobin C• Sickle cell disease• Hemoglobin E• Hemoglobin H disease• Thalassemias• Iron deficiency anemia• Liver disease• Target cells are seen with most of the hemoglobinopathies

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Teardrop cells are commonly seen in:

• Osteopetrosis• Myelofibrosis• Bone marrow infiltrated with hematological or non-hematological malignancies• Iron deficiency anemia• Pernicious anemia• Anemia of renal disease• Artifact of slide preparation

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Basophilic stippling is a collection of fine or coarse granulesin the red cells. Clinically insignificant, fine stippling is often seen in reticulocytes. Coarse stippling is seen in clinically significant conditions with impaired hemoglobin synthesis and is a result of accumulation of abnormal aggregates of ribosomes and polyribosomes.

Basophilic stippling is commonly seen in:• Lead poisoning• Iron deficiency anemia• Thalassemia• Refractory anemia• Congenital hemolytic anemias

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Heinz bodies are multiple blue-purple inclusions attachedto the inner surface of the red cell membrane. They are not visible in Wright-Giemsa-stained blood films, butare visible in supravitally stained smears. Heinz bodies are precipitated normal or unstable hemoglobin usually secondary to oxidant stress.

Heinz bodies are commonly seen in:

• G6PD deficiency• Unstable hemoglobins• Congenital Heinz body (bite cell) anemias

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Howell-Jolly bodies are small round bodies composed of DNA, about 1 μm in diameter, usually single and in the periphery of a red cell.They are readily visible on the Wright-Giemsa-stained smear. The spleen is responsible for the removal of nuclear material in the red cells, so in absence of a functional spleen, nuclear material isremoved ineffectively.

Howell-Jolly bodies are seen in:

• Post splenectomy• Functional asplenia• Anatomical absence of spleen

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Pappenheimer bodies are small dark inclusions 2 to 5 per red cell appearing either singly or in pairs. They are smaller than Howell-Jolly bodies. They are visible on the Wright-Giemsa-stained smear, also stain positive with the Prussian Blue stain, suggestive of presence of iron.

Pappenheimer bodies are seen in iron overload.

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Megaloblast

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Rouleaux formation is a common artifact in the thick area of any blood film. True Rouleaux is seen in the thin part of the blood smear. There are four or more red cells organized in a linear arrangement like a stack of coins.True rouleaux formation is due to increased amounts of plasma proteins primarily fibrinogen and globulins.

Rouleaux are commonly seen in:

• Infections• Inflammation• Monoclonal gammopathies• Neoplastic diseases• AIHA warm antibody disease

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References:

1. Nelson Textbook of Pediatrics

2. Atlas of Pediatric Peripheral Blood Smears (Abbott)

3. hematologyoutlines.com

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