Polychromasia

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Polychromasia
Micrograph showing polychromasia
Synonyms Polychromatophilia
Pronounce N/A
Specialty N/A
Symptoms Anemia, fatigue, pallor
Complications Hypoxia, heart failure
Onset Variable, depending on underlying cause
Duration Variable
Types N/A
Causes Hemolytic anemia, blood loss, bone marrow disorders
Risks Chronic disease, nutritional deficiencies
Diagnosis Blood smear, complete blood count
Differential diagnosis Reticulocytosis, sideroblastic anemia
Prevention Depends on underlying cause
Treatment Address underlying cause, blood transfusion if necessary
Medication N/A
Prognosis Depends on underlying cause
Frequency Common in certain conditions
Deaths N/A


Polychromasia is a medical condition characterized by the presence of polychromatic red blood cells in the blood smear. These cells are typically larger and exhibit a bluish tint when stained with Wright's stain or Giemsa stain, indicating that they are reticulocytes, or immature red blood cells.

Causes[edit]

Polychromasia can be caused by a variety of conditions that lead to increased production of red blood cells by the bone marrow. These conditions include:

Diagnosis[edit]

The diagnosis of polychromasia is typically made through a peripheral blood smear examination. The presence of polychromatic cells is a sign that the bone marrow is responding to an increased demand for red blood cells. Additional tests may include:

Clinical Significance[edit]

Polychromasia is an important diagnostic indicator in various hematological conditions. It suggests active erythropoiesis and can be a response to:

Treatment[edit]

Treatment of polychromasia involves addressing the underlying cause. For instance:

See Also[edit]

References[edit]

External Links[edit]

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