Dyserythropoiesis

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Dyserythropoiesis[edit | edit source]

Iron-deficiency anemia, peripheral blood smear

Dyserythropoiesis refers to the abnormal development of erythrocytes (red blood cells) within the bone marrow. This condition is characterized by ineffective erythropoiesis, leading to various forms of anemia. Dyserythropoiesis can be observed in several hematological disorders and is often associated with morphological abnormalities in erythroid precursors.

Pathophysiology[edit | edit source]

Dyserythropoiesis results from defects in the maturation process of erythroid progenitor cells. These defects can be due to intrinsic abnormalities within the erythroid cells or extrinsic factors affecting the bone marrow environment. The ineffective erythropoiesis leads to increased apoptosis of erythroid precursors, resulting in a reduced number of mature red blood cells entering the circulation.

The morphological abnormalities seen in dyserythropoiesis include:

Clinical Manifestations[edit | edit source]

Patients with dyserythropoiesis typically present with symptoms of anemia, such as fatigue, pallor, and shortness of breath. The severity of symptoms depends on the degree of anemia and the underlying cause of dyserythropoiesis. In some cases, patients may also exhibit signs of hemolysis, such as jaundice and splenomegaly.

Diagnosis[edit | edit source]

The diagnosis of dyserythropoiesis involves a combination of clinical evaluation, laboratory tests, and bone marrow examination. Key diagnostic features include:

  • Complete blood count (CBC) showing anemia with reticulocytopenia.
  • Peripheral blood smear revealing morphological abnormalities in red blood cells.
  • Bone marrow biopsy demonstrating erythroid hyperplasia and dysplastic changes in erythroid precursors.

Treatment[edit | edit source]

The management of dyserythropoiesis focuses on treating the underlying cause and alleviating symptoms of anemia. Treatment options may include:

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Contributors: Prab R. Tumpati, MD