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is a clonal stem cell disorder characterized by excessive proliferation of myeloid cells.
The disease is often without specific symptoms. Often it is detected on a routine full blood count.
Symptoms can include: malaise, low grade fever, increased susceptibility to infections, anemia and thrombocytopenia (although an increased platelet count — thrombocytosis — is often a feature).
CML is often suspected on the basis on the full blood count. When the index of suspicion is high, a bone marrow biopsy is required to distinguish CML from other diseases that feature the same symptoms.
Ultimately, CML is diagnosed by detecting the Philadelphia chromosome (a translocation between the 9th and 22nd chromosome leading to an abberant protein that drives cell division). This translocation leads to bcr-abl fusion and activation of protein tyrosine kinase cascade.
CML occurs in all age groups, but most commonly in the middle-aged and elderly.
Chronic-phase CML is treated with:
In a proportion of patients, the disease remains indolent. In a number, however, it proceeds to accelerated phase and eventually blast crisis, which is virtually indistinguishable from acute myelogenous leukemiaAcute myelogenous leukemia AML is also known as Acute Myeloid Leukemia and is specifically a cancer of the myeloid line of white blood cells. It is the most commonly diagnosed type of adult leukemia, and is rare among children. These malignant cells calle and has a very high mortality rate. This stage can most effectively be treated by a bone marrow transplantBone marrow transplantation is a medical procedure that involves stem cell transplantation. The common feature of recipients is a need for blood stem cells. Most recipients are leukemia patients or others who have been exposed to high doses of chemotherap after high-dose chemotherapy.
| Lymphoma ( Hodgkin's disease, NHL) - Leukemia ( ALL, AML, CLL, CML) - Multiple myeloma - MDS - Myelofibrosis - Myeloproliferative disease ( Thrombocytosis, Polycythemia) - Neutropenia |
| Anemia - Hemochromatosis - Sickle-cell anemia - Thalassemia - other hemoglobinopathies |
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Coagulation and Platelets |
| Thrombosis - Deep venous thrombosis - Pulmonary embolism - Hemophilia - ITP - TTP |