Blood Abnormalities: Insights on Anemia and Other Concerns - Cardiology

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Blood abnormalities


Due to hair loss, I underwent a blood test.
The red blood cell count was normal, but the following results were concerning: hemoglobin at 9.7 g/dL, hematocrit at 31%, mean corpuscular volume (MCV) at 58.4 fL, and mean corpuscular hemoglobin (MCH) at 18.3 pg, all significantly below the standard values.
Additionally, my platelet count was elevated at 425 K/uL, and my white blood cell count was also high at 11,961/uL.
I am unsure of the cause of these abnormalities.
I have a history of thalassemia, and although I consulted my doctor, they mentioned that my results are still too low despite my condition.
This has left me with many questions and concerns about my health.
I also tried iron supplementation for my thalassemia, but it did not help.
I would like to seek guidance from a doctor regarding these issues.
Thank you.

Bobo, 10~19 year old female. Ask Date: 2017/11/01

Dr. He Dongjin reply Cardiology


Hello, the numbers for Mediterranean anemia should be fine if you are regularly being monitored by a hematologist.
Changhua Hospital cares about you.

Reply Date: 2017/11/01

More Info


Understanding blood abnormalities, particularly in the context of anemia and other hematological concerns, can be quite complex. Based on the information provided, it appears that you are experiencing several abnormalities in your blood test results, particularly concerning hemoglobin levels, hematocrit, and other red blood cell indices, alongside elevated white blood cell and platelet counts.


Anemia and Its Types
Anemia is a condition characterized by a deficiency in the number or quality of red blood cells (RBCs), which can lead to reduced oxygen transport in the body. The most common types of anemia include:
1. Iron Deficiency Anemia: This is caused by a lack of iron, which is essential for hemoglobin production. Symptoms may include fatigue, weakness, and pallor.

2. Thalassemia (Mediterranean Anemia): This is a genetic disorder that affects hemoglobin production. Individuals with thalassemia may have low hemoglobin levels and may require regular blood transfusions.

3. Aplastic Anemia: This is a rare but serious condition where the bone marrow fails to produce adequate amounts of blood cells, leading to anemia, increased risk of infections, and bleeding.

4. Megaloblastic Anemia: Often due to vitamin B12 or folate deficiency, this type of anemia is characterized by the production of large, immature red blood cells.


Your Blood Test Results
From your blood test results, the following points stand out:
- Hemoglobin (9.7 g/dL): This is below the normal range, indicating anemia.

- Hematocrit (31%): This is also low, supporting the diagnosis of anemia.

- Mean Corpuscular Volume (MCV) (58.4 fL): This is significantly low, suggesting microcytic anemia, which is often associated with iron deficiency or thalassemia.

- Mean Corpuscular Hemoglobin (MCH) (18.3 Pg): This is low, indicating that the average amount of hemoglobin per red blood cell is reduced.

- Elevated Platelets (425K/uL): This could indicate a reactive process, possibly due to inflammation or another underlying condition.

- Elevated White Blood Cells (11,961/uL): This may suggest an infection, inflammation, or other hematological issues.


Concerns Regarding Mediterranean Anemia
Given your history of Mediterranean anemia (thalassemia), it is crucial to understand how this condition interacts with your current blood abnormalities. Thalassemia can lead to chronic anemia, and individuals with this condition often have a unique blood profile. The presence of low hemoglobin and hematocrit levels, combined with your thalassemia, suggests that your body may be struggling to produce adequate red blood cells.


Recommendations
1. Consult a Hematologist: Given the complexity of your blood results and the presence of thalassemia, it is advisable to consult a hematologist. They can provide a comprehensive evaluation and may recommend further testing, such as hemoglobin electrophoresis, to better understand your specific type of thalassemia and its implications.

2. Iron Supplementation: While you mentioned that iron supplementation has not been effective, it is essential to ensure that you are taking the correct dosage and form of iron. Some individuals with thalassemia may not respond well to iron supplements due to the nature of their condition.

3. Monitor Symptoms: Keep track of any symptoms you experience, such as fatigue, weakness, or shortness of breath. This information can be valuable for your healthcare provider in assessing your condition.

4. Lifestyle Modifications: Ensure you maintain a balanced diet rich in vitamins and minerals, particularly those that support blood health, such as vitamin B12, folate, and iron. Regular check-ups and blood tests can help monitor your condition over time.

5. Addressing Elevated WBC and Platelets: The elevated white blood cell and platelet counts should also be evaluated. These could be indicative of an underlying infection or inflammatory process, and further investigation may be warranted.


Conclusion
Your concerns regarding your blood test results are valid, and it is essential to seek professional medical advice to address these abnormalities. A hematologist will be best equipped to provide a thorough evaluation and tailored treatment plan based on your specific needs and medical history. Remember, managing blood disorders often requires a multi-faceted approach, including medical treatment, lifestyle changes, and regular monitoring.

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