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What is AML?

Acute Myeloid Leukemia (AML) is a type of cancer that affects the blood and bone marrow, causing the bone marrow to produce abnormal white blood cells.

How is AML diagnosed?

AML (Acute Myeloid Leukemia) is typically diagnosed through a combination of medical history evaluation, physical examination, blood tests, and bone marrow biopsy. The doctor may order additional tests such as imaging scans and genetic testing to determine the type and extent of the cancer. The bone marrow biopsy involves taking a small sample of bone marrow and examining it under a microscope to look for abnormal cells. AML is classified based on the type of cells affected and other factors,

What is the cost of AML treatment?

The cost of AML treatment can vary widely depending on the type of treatment required, the duration of treatment, and the location of the hospital.

USD 9647 TO 12863

Who is the right doctor to consult for AML?

An oncologist, who specializes in the treatment of cancer, is the right doctor to consult for AML.

What technology is used during AML treatment?

Flow cytometry: a laboratory technique used to analyze cells and determine the type of cancer cells present in the blood or bone marrow.

PCR (polymerase chain reaction): a lab technique used to identify specific genetic mutations that are associated with AML.

Immunohistochemistry: a lab technique used to identify specific proteins in cancer cells that may be targeted with certain treatments.

PET-CT scans: imaging tests that can detect small areas of cancer activity.

What precautions should be taken during AML treatment?
  • Practice good hygiene to avoid infections.
  • Avoid contact with sick individuals.
  • Take all medications as prescribed by the doctor.
  • Get plenty of rest and maintain a healthy diet.
What are the key tests during AML treatment?
  • Blood tests monitor the number of cancer cells and the patient's overall blood counts.
  • Bone marrow biopsy to determine the extent of the cancer and monitor the effectiveness of treatment.
  • Imaging tests such as X-rays, CT scans, or MRIs may be used to monitor the progression of the disease.

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Frequently Asked Questions

Yes, congenital heart disease can be passed down from a parent to a child. If one or both parents have a congenital heart defect, there is an increased risk of their child having the condition as well. However, it is important to note that not all congenital heart defects are inherited and some can occur due to other factors such as infections during pregnancy or exposure to certain medications or substances.

The initial treatment process for a child with congenital heart disorder depends on the type and severity of the condition. This could include medications for visible symptoms and monitoring with regular checkups.

The tests for congenital heart disorders do not always require hospitalization. Many of the tests can be performed on an outpatient basis, which means the patient can leave the hospital or clinic on the same day. However, some tests may require a short hospital stay, particularly if the patient is an infant or young child.

The treatment options for congenital heart disease may depend on the type and severity of the condition. These options may include medications or procedures like cardiac catheterization.