Can Mediterranean Anemia and Microcytic Anemia Occur Together? - Internal Medicine

Share to:

Mediterranean anemia and microcytic anemia?


Hello, doctor.
Can a person have both thalassemia and microcytic anemia at the same time? I previously took iron supplements and consumed a lot of meat for at least six months, which raised my hemoglobin to normal levels.
However, after stopping the iron supplements, my hemoglobin dropped below 7 again despite a normal diet.
Is this simply due to iron deficiency, or do I need to take iron supplements for life? Thank you for answering my questions.

123, 30~39 year old female. Ask Date: 2021/12/19

Dr. Hong Yuanbin reply Internal Medicine


Hello, microcytic anemia is a general term that encompasses various types of anemia, with the most common being iron deficiency anemia and thalassemia.
To determine which specific type of anemia you have, further testing is required.
For instance, iron deficiency anemia can be assessed through tests for serum iron and ferritin levels.
Thank you for your question.

Reply Date: 2021/12/19

More Info


Mediterranean anemia, also known as thalassemia, and microcytic anemia can indeed occur together in a patient. To understand this better, it's important to first define both conditions.

Mediterranean anemia (thalassemia) is a genetic blood disorder characterized by reduced production of hemoglobin, which is essential for carrying oxygen in the blood. This condition can lead to anemia, as the body does not produce enough healthy red blood cells. There are different types of thalassemia, including alpha and beta thalassemia, which can vary in severity.

Microcytic anemia, on the other hand, is a type of anemia where the red blood cells are smaller than normal (microcytic) and often results from iron deficiency. Iron is a critical component of hemoglobin, and a deficiency can lead to decreased hemoglobin production, resulting in anemia. Microcytic anemia is commonly associated with conditions such as iron deficiency anemia, chronic disease, and sometimes thalassemia.

In your case, it is possible that you are experiencing both conditions simultaneously. If you have a genetic predisposition to thalassemia, your body may have difficulty producing adequate hemoglobin despite your iron intake. This could explain why your hemoglobin levels improved with iron supplementation but dropped again after discontinuation.
The fact that you were able to raise your hemoglobin levels to normal with iron supplements suggests that iron deficiency is a contributing factor to your anemia. However, if you have thalassemia, your body may still struggle to maintain normal hemoglobin levels without ongoing iron supplementation or other treatments.
It is also important to note that excessive iron intake can lead to iron overload, which can be harmful, especially in individuals with thalassemia. Therefore, it is crucial to monitor your iron levels and overall health closely.
In summary, it is possible to have both Mediterranean anemia and microcytic anemia at the same time. Your situation may require a comprehensive evaluation by a hematologist to determine the underlying causes of your anemia and to develop an appropriate treatment plan. This may include ongoing iron supplementation, regular monitoring of hemoglobin levels, and possibly other interventions depending on the severity of your condition and any genetic factors involved.

If you find that your hemoglobin levels continue to drop despite a normal diet and iron supplementation, it may be necessary to explore other treatment options or investigate further for any underlying conditions that could be contributing to your anemia. Always consult with your healthcare provider for personalized advice and treatment options tailored to your specific health needs.

Similar Q&A

Understanding Mediterranean Anemia: Key Lab Values and Implications

WBC 6.25, RBC 5.26, HGB 13.2, HCG 40.6, MCV 77.2, MCH 25.1, MCHC 32.5, PLT 341.0, RDW_CV 19.7, Iron & TIBC: Iron 24, UIBC 369, FE/TIBC 6.5, Ferritin 35. Please check for any abnormalities.


Dr. Lin Shunfa reply Internal Medicine
To Rose: Based on the test data, there may sometimes be errors in the computer input. HGB 13.2: no anemia. MCV 77.2: microcytic, MCH 25.1: low. Iron 24: low iron, low TIBC, low ferritin. RDW-CV 19.7: elevated. If anemia is present, the likelihood of iron deficiency anemia is the ...

[Read More] Understanding Mediterranean Anemia: Key Lab Values and Implications


Understanding Mediterranean Anemia: Key Blood Test Indicators

Hello doctor, I received my military service medical examination report. The white blood cell count (WBC) is 6.6 x 10^3/µL, red blood cell count (RBC) is 6.51 x 10^6/µL, hemoglobin (Hb) is 13.4 g/dL, hematocrit (Hct) is 43.0%, and mean corpuscular volume (MCV) is 65.9 fL. Is ther...


Dr. Hong Yuanbin reply Internal Medicine
Hello, it is indeed possible, but Mediterranean anemia can only be confirmed through further testing. Thank you for your inquiry.

[Read More] Understanding Mediterranean Anemia: Key Blood Test Indicators


Understanding Mediterranean Anemia: Blood Test Insights and Next Steps

Hello, based on my blood test report, is it possible that I have Mediterranean anemia? What is the likelihood? Or what additional tests should I undergo? Thank you. RBC: 5.28 (Male: 4.2-6.2; Female: 3.7-5.5) MIL/cumm Hemoglobin: 13.2 (Male: 12.3-18.3; Female: 11.3-15.3) gm/dL...


Dr. Xiao Yongxun reply Internal Medicine
1. The complete blood count and hemoglobin electrophoresis tests you provided should ideally be ordered by a physician, who should also provide a thorough discussion and explanation of the results. If you have any further questions, please be sure to discuss them with your physic...

[Read More] Understanding Mediterranean Anemia: Blood Test Insights and Next Steps


Understanding Mediterranean Anemia: Causes and Symptoms Explained

I learned about the possibility of having a condition due to a health check, so I would like to understand the causes and symptoms first.


Dr. Lin Mingxing reply Family Medicine
Mediterranean anemia, also known as thalassemia, is a congenital genetic disorder characterized by microcytic anemia, which means that the red blood cells are smaller in size and more fragile, leading to impaired function and increased susceptibility to destruction. The lifespan ...

[Read More] Understanding Mediterranean Anemia: Causes and Symptoms Explained


Related FAQ

Anemia

(Internal Medicine)

Anemia

(Cardiology)

White Blood Cells

(Internal Medicine)

Blood

(Gastroenterology and Hepatology)

Platelets

(Internal Medicine)

Bacteremia

(Internal Medicine)

Hemoglobin A1C

(Internal Medicine)

Hepatitis C

(Internal Medicine)

Anemia

(Oncology)

Autoimmune Disease

(Internal Medicine)