Chronic myeloid leukemia: Difference between revisions

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*Triphasic: chronic phase, accelerated phase, and blast crisis
*Triphasic: chronic phase, accelerated phase, and blast crisis
*Almost half are asymptomatic on diagnosis
*Almost half are asymptomatic on diagnosis, found by abnormalities on routine bloodwork
*Presenting complaints may include fatigue, weight loss, sweating, abdominal fullness, and bleeding
*Presenting complaints may include fatigue, weight loss, sweating, abdominal fullness, and bleeding
*Often have [[splenomegaly]], which can contribute to the abdominal fullness and cause LUQ or left shoulder pain
*Often have [[splenomegaly]], which can contribute to the abdominal fullness and cause LUQ or left shoulder pain
*Can present with anemia, very elevated WBCs, and elevated platelets
*Can present with anemia, very elevated WBCs, and elevated platelets
*Can precipitate [[gout]]
*Extramedullary findings are usually limited to blast crisis, and would include lymphadenopathy, skin findings, and soft tissue findings


=== Prognosis and Complications ===
===Prognosis and Complications===


* Outcomes are very good since the introduction of tyrosine kinase inhibitors
*Outcomes are very good since the introduction of tyrosine kinase inhibitors
* Prognostic models exist, including Sokal, Euro (Hasford), EUTOS, and ELTS scores
*Prognostic models exist, including [[Sokal score]], Euro (Hasford), EUTOS, and ELTS scores


== Differential Diagnosis ==
==Differential Diagnosis==


* [[Leukemoid reaction]]
*[[Leukemoid reaction]]
* [[Juvenile myelomonocytic leukemia]]
*[[Juvenile myelomonocytic leukemia]]
* [[Chronic myelomonocytic leukemia]]
*[[Chronic myelomonocytic leukemia]]
* [[Chronic eosinophilic leukemia]]
*[[Chronic eosinophilic leukemia]]
* [[Chronic neutrophilic leukemia]]
*[[Chronic neutrophilic leukemia]]


== Diagnosis ==
==Diagnosis==


* Usually suspected in asymptomatic patient with typical findings in peripheral blood or bone marrow
*Usually suspected in asymptomatic patient with typical findings in peripheral blood or bone marrow
* Confirmed with detection of BCR-ABL1 fusion gene in peripheral blood or bone marrow
*Confirmed with detection of BCR-ABL1 fusion gene in peripheral blood or bone marrow


== Management ==
==Management==


* Can use empiric [[hydroxyurea]] for cytoreduction while awaiting diagnosis if WBC >80
*Can use empiric [[hydroxyurea]] for cytoreduction while awaiting diagnosis if WBC >80


[[Category:Hematology]]
[[Category:Hematology]]

Latest revision as of 14:34, 20 February 2022

Clinical Manifestations

  • Triphasic: chronic phase, accelerated phase, and blast crisis
  • Almost half are asymptomatic on diagnosis, found by abnormalities on routine bloodwork
  • Presenting complaints may include fatigue, weight loss, sweating, abdominal fullness, and bleeding
  • Often have splenomegaly, which can contribute to the abdominal fullness and cause LUQ or left shoulder pain
  • Can present with anemia, very elevated WBCs, and elevated platelets
  • Can precipitate gout
  • Extramedullary findings are usually limited to blast crisis, and would include lymphadenopathy, skin findings, and soft tissue findings

Prognosis and Complications

  • Outcomes are very good since the introduction of tyrosine kinase inhibitors
  • Prognostic models exist, including Sokal score, Euro (Hasford), EUTOS, and ELTS scores

Differential Diagnosis

Diagnosis

  • Usually suspected in asymptomatic patient with typical findings in peripheral blood or bone marrow
  • Confirmed with detection of BCR-ABL1 fusion gene in peripheral blood or bone marrow

Management

  • Can use empiric hydroxyurea for cytoreduction while awaiting diagnosis if WBC >80