Acute myeloid dendritic cell leukemia

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Acute myeloid dendritic cell leukemia (AMDL) is a rare subtype of leukemia, a group of cancers that generally begin in the bone marrow and result in high numbers of abnormal white blood cells. Specifically, AMDL is a form of acute myeloid leukemia (AML), which is characterized by the rapid growth of abnormal cells that build up in the bone marrow and blood and interfere with normal blood cell production.

Etiology[edit | edit source]

The exact cause of AMDL is unknown, but it is believed to be related to genetic mutations. These mutations can be inherited or acquired during a person's lifetime. Some studies suggest that exposure to certain chemicals or radiation may increase the risk of developing AMDL.

Pathophysiology[edit | edit source]

In AMDL, the myeloid dendritic cells, which are a type of immune cell, become cancerous. These cells are responsible for presenting antigens to the T cells to initiate an immune response. When these cells become cancerous, they proliferate uncontrollably and crowd out the healthy cells in the bone marrow.

Clinical Presentation[edit | edit source]

Patients with AMDL may present with symptoms similar to other forms of leukemia, such as fatigue, fever, weight loss, and frequent infections. They may also have an enlarged spleen or liver, and may experience bleeding or bruising easily.

Diagnosis[edit | edit source]

Diagnosis of AMDL is based on a combination of clinical symptoms, blood tests, and bone marrow biopsy. The presence of abnormal myeloid dendritic cells in the blood or bone marrow is a key diagnostic feature of AMDL.

Treatment[edit | edit source]

Treatment for AMDL typically involves chemotherapy to kill the cancer cells, followed by a stem cell transplant to replace the damaged bone marrow. However, the prognosis for patients with AMDL is generally poor, with a high risk of relapse.

See Also[edit | edit source]

Template:Leukemia

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Contributors: Prab R. Tumpati, MD