Aplastic anemia is a rare but serious condition in which the bone marrow fails to produce enough blood cells, including red blood cells, white blood cells, and platelets. This can lead to fatigue, infections, and excessive bleeding. The condition can develop suddenly or gradually and may be life-threatening if left untreated.
Aplastic anemia occurs when the bone marrow is damaged, leading to reduced blood cell production. Common causes include:
Autoimmune disorders – The immune system mistakenly attacks bone marrow stem cells.
Exposure to toxic chemicals – Pesticides, benzene, and other harmful substances can damage the bone marrow.
Radiation and chemotherapy – Cancer treatments may harm bone marrow cells.
Certain medications – Some antibiotics and nonsteroidal anti-inflammatory drugs (NSAIDs) may contribute to bone marrow suppression.
Viral infections – Hepatitis, Epstein-Barr virus (EBV), and HIV may trigger aplastic anemia.
Genetic disorders – Some inherited conditions, such as Fanconi anemia, increase the risk.
Symptoms of aplastic anemia can vary in severity and may include:
Fatigue and weakness
Frequent infections due to low white blood cells
Unusual or prolonged bleeding, including nosebleeds and gum bleeding
Easy bruising
Shortness of breath
Pale skin
Dizziness or headaches
At Vibhavadi Hospital, our specialists use cutting-edge diagnostic tools to accurately identify aplastic anemia:
Measures the levels of red blood cells, white blood cells, and platelets.
A small sample of bone marrow is taken and examined to determine the extent of blood cell production failure.
Checks for viral infections, autoimmune diseases, or toxic exposures that may contribute to aplastic anemia.
Identifies inherited conditions linked to aplastic anemia.
Red blood cell transfusions: Help relieve anemia-related symptoms like fatigue.
Platelet transfusions: Prevent excessive bleeding in patients with low platelet counts.
Antithymocyte Globulin (ATG) and Cyclosporine: Suppress the immune system to stop it from attacking bone marrow cells.
Eltrombopag (Promacta): Stimulates the bone marrow to produce more blood cells.
Corticosteroids: Sometimes used to reduce immune system activity.
The most effective long-term treatment, especially for younger patients or those with severe aplastic anemia.
Requires a compatible donor, usually a sibling or unrelated matched donor.
Medications like granulocyte-colony stimulating factor (G-CSF) encourage white blood cell production to prevent infections.
If a virus, medication, or toxic exposure is the cause, treatment involves eliminating the trigger.
Our highly experienced hematologists and oncologists specialize in diagnosing and treating blood disorders, including aplastic anemia.
We offer advanced therapies, including immunosuppressive treatments, stem cell transplants, and targeted medications.
Our hospital is equipped with modern diagnostic and treatment technologies to ensure accurate detection and effective management of aplastic anemia.
We provide tailored treatment plans based on each patient’s condition, age, and treatment response.
Our team includes psychologists, nutritionists, and rehabilitation specialists to support patients throughout their treatment journey.
To consult with our Hematology Specialists, you can book an appointment through:
Phone Call: Contact our hospital hotline.
Online Booking: Visit our official website https://www.vibhavadi.com/th.
Walk-In Visits: Available at our Hematology Department.
We accept various health insurance plans, and our patient service team can assist with treatment cost estimates and payment plans.
Aplastic anemia is a serious but treatable condition. With early diagnosis and appropriate medical care, patients can manage their symptoms and lead healthy lives. At Vibhavadi Hospital, our expert hematologists provide advanced treatments tailored to each patient’s needs. Contact us today to schedule a consultation and learn more about our specialized care options.
A1: No, aplastic anemia is not cancer, but it is a serious blood disorder that affects bone marrow function.
A2: In some cases, a bone marrow transplant can cure aplastic anemia. Other treatments, such as immunosuppressive therapy, can help manage the condition.
A3: Some cases are inherited (such as Fanconi anemia), but most are acquired due to autoimmune reactions, infections, or environmental factors.
A4: The prognosis depends on treatment response. With proper treatment, many patients live long and healthy lives.
A5: Yes, avoiding infections, maintaining a balanced diet, and following medical advice can improve overall health and treatment success.
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