Chronic myelogenous leukemia
(Redirected from Chronic myeloid leukemia)
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Chronic myelogenous leukemia | |
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Synonyms | N/A |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Fatigue, weight loss, fever, night sweats, splenomegaly |
Complications | Blast crisis, anemia, thrombocytopenia |
Onset | Typically in adulthood |
Duration | Chronic |
Types | N/A |
Causes | Philadelphia chromosome (translocation between chromosome 9 and chromosome 22) |
Risks | Radiation exposure, age, male gender |
Diagnosis | Complete blood count, bone marrow biopsy, cytogenetic analysis |
Differential diagnosis | Chronic lymphocytic leukemia, acute myeloid leukemia, myeloproliferative neoplasms |
Prevention | N/A |
Treatment | Tyrosine kinase inhibitors, chemotherapy, stem cell transplant |
Medication | N/A |
Prognosis | Generally good with treatment |
Frequency | 1-2 cases per 100,000 people per year |
Deaths | N/A |
Chronic myelogenous leukemia (CML), also known as chronic myeloid leukemia, is a type of cancer that originates in the bone marrow and results in the overproduction of white blood cells. It is a form of leukemia, which is a group of cancers that typically begin in the bone marrow and result in high numbers of abnormal white blood cells.
Pathophysiology
CML is characterized by the presence of the Philadelphia chromosome, a specific genetic abnormality in chromosome 22 of human cells. This abnormality is a result of a translocation between chromosome 9 and chromosome 22, which creates the BCR-ABL fusion gene. The BCR-ABL gene produces a protein with tyrosine kinase activity that leads to uncontrolled cell division.
Symptoms
Common symptoms of CML include:
- Fatigue
- Weight loss
- Night sweats
- Fever
- Splenomegaly (enlarged spleen)
- Hepatomegaly (enlarged liver)
- Bone pain
Diagnosis
CML is typically diagnosed through a combination of blood tests, bone marrow biopsy, and cytogenetic analysis. The presence of the Philadelphia chromosome is a key diagnostic marker.
Stages
CML progresses through three phases:
- Chronic phase: The disease progresses slowly and patients may have mild symptoms.
- Accelerated phase: The disease progresses more rapidly and symptoms become more severe.
- Blast crisis: The disease behaves like an acute leukemia with rapid progression and severe symptoms.
Treatment
Treatment options for CML include:
- Tyrosine kinase inhibitors (TKIs) such as imatinib, dasatinib, and nilotinib.
- Chemotherapy
- Stem cell transplant
- Interferon therapy
Prognosis
The prognosis for CML has improved significantly with the advent of tyrosine kinase inhibitors. Many patients achieve long-term remission and have a normal life expectancy.
Epidemiology
CML accounts for about 15-20% of all cases of adult leukemia. It is more common in older adults, with the median age at diagnosis being around 65 years.
See also
References
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Contributors: Prab R. Tumpati, MD