Acute basophilic leukemia

Acute basophilic leukemia
Synonyms
Pronounce	N/A
Specialty	N/A
Symptoms	Fatigue (medical), fever, easy bruising, bleeding, anemia, infections
Complications	Disseminated intravascular coagulation, organ failure
Onset
Duration
Types
Causes	Genetic mutations
Risks
Diagnosis	Bone marrow biopsy, blood test
Differential diagnosis	Chronic myeloid leukemia, acute myeloid leukemia, acute lymphoblastic leukemia
Prevention
Treatment	Chemotherapy, stem cell transplant
Medication
Prognosis
Frequency	Rare
Deaths	N/A

Acute Basophilic Leukemia Acute Basophilic Leukemia (ABL) is a rare and aggressive form of acute myeloid leukemia (AML) characterized by the proliferation of immature basophilic granulocytes. This condition is marked by the presence of basophilic blasts in the bone marrow and peripheral blood, leading to a rapid progression of symptoms and requiring prompt medical intervention.

Pathophysiology

ABL is a subtype of AML, which is a cancer of the blood and bone marrow. In ABL, there is an abnormal increase in basophilic precursors, which are immature white blood cells that normally develop into basophils. Basophils are a type of granulocyte involved in inflammatory responses and allergic reactions. The overproduction of these immature cells disrupts normal hematopoiesis, leading to a deficiency of normal blood cells.

Clinical Presentation

Patients with ABL typically present with symptoms related to bone marrow failure, such as anemia, thrombocytopenia, and neutropenia. Common symptoms include fatigue, easy bruising or bleeding, and increased susceptibility to infections. Additionally, patients may experience symptoms related to the infiltration of basophilic blasts in various organs, such as skin rashes or gastrointestinal disturbances.

Diagnosis

The diagnosis of ABL involves a combination of clinical evaluation, laboratory tests, and bone marrow examination. Key diagnostic features include:

• Peripheral Blood Smear: Presence of basophilic blasts.
• Bone Marrow Biopsy: Hypercellular marrow with a predominance of basophilic blasts.
• Cytogenetic Analysis: Identification of chromosomal abnormalities, which may include translocations or mutations specific to ABL.
• Immunophenotyping: Flow cytometry to determine the expression of specific cell surface markers characteristic of basophilic lineage.

Treatment

The treatment of ABL is similar to other forms of AML and typically involves intensive chemotherapy. The standard treatment regimen may include:

• Induction Chemotherapy: Aimed at achieving complete remission by reducing the number of leukemic cells.
• Consolidation Therapy: Additional chemotherapy to eliminate residual disease and prevent relapse.
• Stem Cell Transplantation: Considered in eligible patients to provide a potential cure.

Prognosis

The prognosis for patients with ABL is generally poor due to the aggressive nature of the disease and its resistance to standard therapies. Factors influencing prognosis include the patient’s age, overall health, and specific genetic mutations present in the leukemic cells.

Research and Future Directions

Ongoing research is focused on understanding the molecular mechanisms underlying ABL and developing targeted therapies. Advances in genetic profiling and personalized medicine hold promise for improving outcomes in patients with this rare leukemia subtype.

Also see

• Acute myeloid leukemia
• Chronic myeloid leukemia
• Hematopoiesis
• Leukemia
• Stem cell transplantation