Differential Diagnosis for Markedly Elevated WBC + Increased Myeloid Precursors
Single Most Likely Diagnosis
- Chronic Myeloid Leukemia (CML): This condition is characterized by the marked elevation of white blood cell count (WBC) with a left shift, indicating the presence of immature myeloid cells (myeloid precursors) in the peripheral blood. The presence of the Philadelphia chromosome is diagnostic.
Other Likely Diagnoses
- Leukemoid Reaction: A reactive process that mimics leukemia, often seen in response to severe infection, inflammation, or other stressors. It presents with a significantly elevated WBC count and the presence of myeloid precursors but lacks the clonality seen in leukemia.
- Myeloproliferative Neoplasms (MPN): Conditions such as Polycythemia Vera, Essential Thrombocytosis, and Primary Myelofibrosis can present with elevated WBC counts and myeloid precursors due to the overproduction of myeloid cells.
- Acute Myeloid Leukemia (AML): Although AML typically presents with a decrease in normal blood cells, some subtypes can present with an elevated WBC count and myeloid precursors.
Do Not Miss Diagnoses
- Acute Promyelocytic Leukemia (APL): A subtype of AML characterized by the accumulation of promyelocytes. It is critical to diagnose promptly due to its association with severe coagulopathy and the need for specific treatment.
- Sepsis with a Leukemoid Reaction: Sepsis can induce a significant increase in WBC count and the presence of myeloid precursors. Early recognition and treatment of the underlying infection are crucial.
Rare Diagnoses
- Chronic Neutrophilic Leukemia (CNL): A rare myeloproliferative neoplasm characterized by sustained neutrophilia without the Philadelphia chromosome.
- Myelodysplastic Syndromes (MDS): Although MDS often presents with cytopenias, some cases can have a leukemoid reaction or increased myeloid precursors, especially in the context of transformation to AML.
- Juvenile Myelomonocytic Leukemia (JMML): A rare leukemia in children characterized by the proliferation of granulocytic and monocytic precursors.