Management Approach for Leukocytosis
The management of leukocytosis should be directed at identifying and treating the underlying cause, with immediate intervention required for white blood cell counts above 100,000/mm³ due to the risk of brain infarction and hemorrhage. 1
Initial Assessment and Differential Diagnosis
Common Causes of Leukocytosis:
Benign/Secondary Causes (most common):
- Infections
- Inflammatory processes
- Physical or emotional stress
- Medications (corticosteroids, lithium, beta agonists) 1
- Pregnancy
Primary Bone Marrow Disorders (less common but more serious):
- Acute leukemias
- Chronic leukemias
- Myeloproliferative disorders 1
Key Diagnostic Steps:
Complete Blood Count with Differential:
- Determine which leukocyte subpopulation is elevated (neutrophils, lymphocytes, eosinophils, etc.)
- Assess for concurrent abnormalities in red blood cells or platelets 2
Peripheral Blood Smear:
- Look for immature cells or "left shift" (increased band forms)
- Evaluate for toxic granulation (suggests infection rather than stress-induced leukocytosis) 3
Clinical Correlation:
- Presence of fever, infection signs
- Weight loss, bleeding, bruising
- Hepatosplenomegaly or lymphadenopathy
- Immunosuppression history 1
Management Algorithm Based on Cause
1. Hyperleukocytosis (WBC >100,000/mm³)
- Immediate intervention required - medical emergency due to risk of brain infarction and hemorrhage 1
- Management:
- Hydroxyurea at dosages up to 50-60 mg/kg/day until WBC <10-20 × 10⁹/L 4
- Consider leukapheresis for initial management (though no proven impact on long-term outcome) 4
- Avoid excessive red blood cell transfusions until WBC reduced (can increase blood viscosity) 4
- Prevention of tumor lysis syndrome:
- Hydration
- Control of uric acid (allopurinol or rasburicase)
- Monitor urine pH 4
2. Leukocytosis Due to Hematologic Malignancy
Acute Myeloid Leukemia (AML):
Chronic Myelogenous Leukemia (CML):
3. Infection-Related Leukocytosis
- Identify and treat the underlying infection
- Empirical broad-spectrum antimicrobial therapy for febrile neutropenic patients 4
- Consider prophylactic oral antibiotics for prolonged, profound granulocytopenia (<100/mm³ for two weeks) 4
4. Medication-Induced Leukocytosis
- Recognize that even small doses of prednisone can induce extreme and persistent leukocytosis 3
- Distinguish from infection-related leukocytosis by noting:
- Prednisone typically causes <6% band forms
- Toxic granulation is rare in steroid-induced leukocytosis 3
- Consider medication adjustment if clinically appropriate
5. "Unexplained" Leukocytosis
- May represent persistent inflammation-immunosuppression and catabolism syndrome (PICS)
- Often seen in patients with extensive tissue damage rather than active infection
- Cautious use of antibiotics as they may not provide benefit 5
- Monitor for colonization with resistant organisms (e.g., Clostridium difficile) 5
Special Considerations
Leukocytosis in Adult-Onset Still's Disease
- Characterized by striking neutrophilia secondary to bone marrow granulocyte hyperplasia
- 50% of patients may have peripheral leukocyte counts >15×10⁹/L
- 37% may have WBC counts >20×10⁹/L 4
- Often accompanies increased disease activity
Platelet Transfusion Guidelines
- Transfuse if platelet count ≤10 × 10⁹/L
- For counts 10-20 × 10⁹/L, transfuse if fever/infection present
- For counts >20 × 10⁹/L, transfuse only for clinically relevant hemorrhage 4
Red Flags Requiring Urgent Evaluation
- WBC count >100,000/mm³ (medical emergency) 1
- Concurrent abnormalities in red blood cell or platelet counts
- Constitutional symptoms (fever, weight loss, night sweats)
- Hepatosplenomegaly or significant lymphadenopathy
- Abnormal peripheral blood smear with blast cells
Remember that while leukocytosis is often due to benign causes, it can also be the first sign of serious underlying conditions that require prompt diagnosis and treatment.