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Erythroblastic Anemia - Symptoms, Diagnosis, and Treatment

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Anemia with a high number of nucleated red blood cells in the peripheral blood is known as erythroblastic anemia. Read on to know more about it.

Medically reviewed by

Dr. Abdul Aziz Khan

Published At December 5, 2022
Reviewed AtJune 7, 2023

What Is Anemia?

The disc-shaped blood cells, known as red blood cells, transport oxygen to the body's organs and tissues. Anemia occurs when the body's healthy red blood cell count is too low. A decrease in the amount of oxygen delivered to the body's vital organs and tissues is the root cause of many anemia symptoms, including exhaustion and shortness of breath. Red blood cells contain the protein hemoglobin, which is rich in iron. Because hemoglobin binds to oxygen in the lungs, red blood cells. Based on the amount of hemoglobin in the blood, anemia is assessed.

Anemia is typically caused by a combination of factors that either reduce or increase the production of red blood cells. Individuals might not even be aware that they have anemia because the symptoms can be so subtle. As the blood cells start to disappear, symptoms frequently start to appear. Dizziness, lightheadedness, headaches, shortness of breath, cold hands and feet, and pale skin are typical symptoms. The complete blood count (CBC) test, which measures the red blood cells, hemoglobin, and other components of the blood, is typically used to diagnose it. The type of anemia will determine how it is treated. Oxygen, analgesics, and oral and intravenous fluids are frequently given to treat pain and avoid complications.

What Are Erythrocytes?

Erythrocytes are red blood cells. They are mature red blood cells without a nucleus and retain a biconcave (concave on both sides) discoid shape. Gas exchange and transport are erythrocytes' primary functions. They transport oxygen from the lungs to the body's cells and tissues. Additionally, they return carbon dioxide waste products from the cells to the lungs for exhalation. Because of their special disc shape and pliability, erythrocytes can efficiently move through capillaries, the smallest blood vessels, and maximize surface area for maximum gas exchange.

The three stages of erythrocytes' life cycle are production, maturation, and destruction. In the red bone marrow, erythropoiesis, the process by which erythrocytes are produced, is a component of the hematopoiesis process. Colony forming unit -erythroid (CFU-E), an erythroid stem cell, is produced during the first stages of hematopoiesis. This signals the start of the erythropoietin-driven process. In the bone marrow, these cells are located in erythroid islands, where they proliferate and develop into mature RBCs. Erythrocytes, erythroblasts, proerythroblasts, and reticulocytes are the cells that result from the differentiation process. The membrane that covers erythrocytes is made up of proteins and lipids. In the bone marrow, red blood cells are produced by nucleated cells called erythroblasts.

What Is Erythroblastic Anemia?

Cooley distinguished erythroblastic anemia, also known as Mediterranean anemia, thalassemia, or Cooley's anemia, based on racial incidence, from the group of anemias exhibiting the von Jaksch syndrome. Only children of races descended from the Mediterranean region, particularly from Greece and Italy, are affected by the familial disease. It is characterized by slow-moving anemia and high-nucleated red blood cells. The bones, particularly those in the skull, change as a result of the extraordinary proliferation of erythroblast tissue. The first symptom could be an extremely pale complexion with an icteric tint, followed by a protruding belly from splenomegaly. The presence of evidence of cardiac insufficiency may also manifest as these symptoms and signs worsen.

There may be episodes of unexplained fever. In addition, there may be a delay in physical development. There are several characteristics of erythroblastic anemia, including a consistent racial and familial incidence, a characteristic facial appearance, anemia progressing with high nucleated erythrocytes in the peripheral bloodstream, enlarged spleens, distinctive changes in the bones, and, in the end, histologic lesions of the bone marrow and spleen.

Many erythroblasts present in large numbers could have originated from extramedullary foci of erythropoiesis. In myelofibrosis and carcinomatosis, a few granulocyte precursors are also often present, and erythroblast numbers are usually high compared to the severity of anemia.

After splenectomy, erythroblasts are typically found in the peripheral blood, and many of them may be present in cases of severe anemia and extramedullary erythropoiesis. Patients with sickle cell anemia frequently have large numbers on their blood films during severe crises. There are frequently a few erythroblasts in small numbers in the blood of patients with cyanotic heart failure or septicemia.

What Are the Signs and Symptoms of Erythroblastic Anemia?

Patients may experience different signs and symptoms. However, those with these conditions primarily feel the following conditions.

  • Extreme icteric tint to the skin's pallor.

  • Splenomegaly (increased spleen size).

  • Cardiac dysfunction.

  • Episodes of unexplained fever.

  • Delay in physical development.

  • Epicanthus (eyelids that are obliquely or vertically folded inward toward the medial canthus).

  • Mild exophthalmos (bulging of the eyes, which can result in one or both eyes slipping out of their sockets).

How to Diagnose Erythroblastic Anemia?

Erythroblastic anemia can be diagnosed in several ways, but the following are the most typical ones.

  • Complete Blood Count (CBC) - Using this test, medical professionals can examine all of the blood cells, concentrating on the red blood cells. They measure the size and shape of the red blood cells in addition to counting them. This test is used to check the levels of blood contents.

  • Peripheral Blood Smear- Medical professionals examine red blood cells under a microscope to assess them.

How to Treat Erythroblastic Anemia?

The type, cause, and severity of anemia affect how it is treated. Treatments for blood loss may include dietary adjustments or supplements, medications, procedures, or surgery.

  • To treat an iron deficiency, use iron supplements.

  • Low vitamin levels may be treated with vitamin B supplements.

  • In the case of blood loss, blood transfusions may be administered.

  • Medication to stimulate blood formation may be used if the body produces less blood.

Conclusion

Erythroblastic anemia is a type of anemia that is characterized by the presence of a lot of nucleated red blood cells in the peripheral blood (both normoblasts and erythroblasts). ABO or Rh incompatibility can lead to isoimmunization, which is seen in newborns with hemolytic anemia. Although the disease has a progressive course, some patients may live into adulthood. Periods of hyperpyrexia occasionally occur without any other signs of infection. However, infection is typically fatal.

Frequently Asked Questions

1.

Is Erythroblastic Anemia a Genetic Disorder?

Erythroblastic anemia can be caused by both genetic and non-genetic factors. Some forms of the disorder are autosomal recessive, which means that two duplicates of the defective gene are required to develop the disorder. Other forms may be acquired due to environmental factors such as infectious diseases, nutritional deficiencies, or toxicity exposure.

2.

What Occurs in the Erythroblast?

Erythroblasts are developing red blood cells in the bone marrow. Erythroblasts synthesize and accumulate hemoglobin, the protein that allows red blood cells to carry oxygen, during development. They also lose their organelles, including the nucleus, allowing them to carry more hemoglobin and have a distinctive biconcave shape. When erythroblasts reach full maturity, they are circulated as functional red blood cells.

3.

What Is the Location of the Erythroblast?

Erythroblasts are found in bone marrow, the smooth, spongy tissue within bone cavities. The bone marrow produces red blood cells, white blood cells, and platelets, and erythroblasts are the precursors to red blood cells.

4.

What Is the Distinction Between an Erythrocyte and an Erythroblast?

Erythrocytes, or red blood cells, are mature cells in the bloodstream that transport oxygen to tissues throughout the body. Erythroblasts, conversely, are immature bone marrow cells that give rise to erythrocytes. As they mature into erythrocytes, erythroblasts synthesize and accumulate hemoglobin, the protein that allows red blood cells to carry oxygen, and gradually lose their organelles, including the nucleus.

5.

What Exactly Is Red Blood Count in Thalassemia?

RBC (red blood cell) production is impaired in thalassemia due to abnormal or reduced synthesis of hemoglobin, the protein in RBCs that transports oxygen. As a result, the number of RBCs decreases, they become smaller and paler, and their ability to carry oxygen decreases. The type and number of mutations in the genes that control hemoglobin synthesis determine the severity of the condition.

6.

Which Anaemia Is Associated With Thalassemia?

Thalassemia is a group of inherited blood disorders that can result in anemia of various types, including alpha and beta-thalassemia and other rare forms. The type and number of mutations in the genes that control hemoglobin production determine the severity of anemia in thalassemia.

7.

Erythroblastosis Occurs Under What Circumstances?

Erythroblastosis fetalis, also known as hemoglobin concentration in the newborn, occurs when a mother's and her fetus' blood types are incompatible. This can occur when an Rh-negative mother carries an Rh-positive fetus, resulting in severe anemia and other complications for the unborn baby.

8.

Which Type of Thalassemia Is the Most Severe?

The most severe form of thalassemia is beta thalassemia major, also known as Cooley's anemia. Genetic changes in both duplicates of the HBB gene, which codes for beta-globin, result in reduced or absent hemoglobin production. Life-threatening complications of beta thalassemia major include severe anemia, bone deformities, and organ damage.

9.

Which Type of Thalassemia Cannot Be Cured?

Cooley's anemia, also known as beta-thalassemia major, is incurable. It is a genetic disorder that affects hemoglobin production and necessitates lifelong management. Blood transfusions, iron chelation therapy, and stem cell transplantation are all treatment options for beta-thalassemia major, but there is currently no cure.

10.

What’s Another Term for Erythroblast?

A normoblast is another name for an erythroblast. Both terms refer to the immature stage of red blood cell development in the bone marrow, characterized by hemoglobin synthesis and the progressive loss of the nucleus and organelles.

11.

Is It Possible to Find Erythroblasts in Bone Marrow?

Erythroblasts can be found in the bone marrow. They are the immature precursor cells of red blood cells that synthesize and accumulate hemoglobin. Erythroblasts lose their nucleus and other organelles as they mature, becoming mature red blood cells that are released into the bloodstream.

12.

Where Do Erythroblasts Develop?

Erythroblasts form in bone marrow, the spongy tissue found inside bone cavities. They develop from hematopoietic stem cells and undergo maturation stages before being released into the bloodstream as mature red blood cells.

13.

What is the treatment for Erythroblastosis?

The severity of the condition determines the treatment for erythroblastosis fetalis, also known as hemolytic disease of the newborn. Mild cases may not necessitate treatment, whereas severe cases may necessitate fetal blood transfusions, premature delivery, or other interventions. To prevent erythroblastosis in future pregnancies, Rh immunoglobulin injections are given.

14.

Is the Rood Blood Count Elevated in Thalassemia?

The bone marrow's attempt to compensate for the decreased hemoglobin production can cause an increase in RBC count in thalassemia. However, the number of red blood cells in the body may still be insufficient to deliver enough oxygen to the tissues, resulting in anemia and other complications.
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Dr. Abdul Aziz Khan
Dr. Abdul Aziz Khan

Medical oncology

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