Treatment of Leukocytosis
The treatment of leukocytosis should be directed at the underlying cause rather than the elevated white blood cell count itself, with specific interventions determined by the etiology and severity of the condition. 1
Diagnostic Approach to Leukocytosis
Before initiating treatment, it's essential to determine:
- Which leukocyte subpopulation is elevated (neutrophils, lymphocytes, eosinophils, etc.)
- Whether there are concurrent abnormalities in red blood cells or platelets
- The presence of any symptoms suggesting a specific underlying condition
Common Causes of Leukocytosis
Reactive causes (most common):
- Infections (bacterial, viral, fungal)
- Inflammation
- Physical or emotional stress
- Medications (corticosteroids, lithium, beta-agonists)
Primary bone marrow disorders:
- Leukemias (acute and chronic)
- Myeloproliferative disorders
Treatment Algorithm Based on Cause
1. Infection-Related Leukocytosis
- Identify the source of infection through appropriate cultures and imaging
- Administer targeted antimicrobial therapy based on suspected or confirmed pathogens
- For febrile neutropenia, empiric broad-spectrum antimicrobial therapy is recommended 1
2. Inflammatory Conditions
- Treat the underlying inflammatory condition (e.g., autoimmune disorders, tissue injury)
- Anti-inflammatory medications may be indicated based on the specific condition
3. Medication-Induced Leukocytosis
- Consider dose reduction or discontinuation of the offending medication if clinically appropriate
- Monitor WBC counts after medication adjustment
4. Leukemia and Myeloproliferative Disorders
Acute Myeloid Leukemia (AML)
- Induction chemotherapy with cytarabine and an anthracycline (daunorubicin, idarubicin, or mitoxantrone) 2, 1
- Treatment should be conducted in specialized centers with adequate multidisciplinary infrastructure 2
Chronic Myelogenous Leukemia (CML)
- Tyrosine kinase inhibitors (e.g., imatinib) are the standard of care 1
- For symptomatic leukocytosis in CML, hydroxyurea, apheresis, imatinib, or clinical trial participation are recommended 2
Chronic Lymphocytic Leukemia (CLL)
- Treatment decisions should be based on disease stage, previous treatments, and genetic factors 2
- Patients should be stratified based on whether they have leukemia cells with del(17p) or del(11q) 2
Management of Severe Leukocytosis
For WBC counts >100,000/μL (medical emergency)
- Leukapheresis should be considered for immediate reduction of WBC count due to risk of brain infarction and hemorrhage 1, 3
- Hydroxyurea at dosages up to 50-60 mg/kg/day until WBC <10-20 × 10⁹/L 1
- Avoid excessive red blood cell transfusions until WBC is reduced, as this can increase blood viscosity 1
Prevention of Tumor Lysis Syndrome
- Aggressive hydration
- Control of uric acid (allopurinol or rasburicase)
- Monitoring of urine pH and electrolytes 1
Special Considerations
Unexplained Persistent Leukocytosis
- Often seen in hospitalized patients with extensive tissue damage rather than active infection
- May represent persistent inflammation-immunosuppression and catabolism syndrome (PICS)
- Prudent use of antibiotics is recommended, as prolonged empiric broad-spectrum antibiotics may not be beneficial 4
Paraneoplastic Leukocytosis
- Can occur in solid tumors (e.g., thyroid anaplastic carcinoma) due to cytokine secretion
- Treatment should focus on the underlying malignancy 5
Follow-up and Monitoring
- Regular complete blood counts with differential to monitor response to treatment
- Bone marrow examination may be necessary for suspected primary bone marrow disorders
- Response evaluation should include clinical examination and serial peripheral blood counts 2
Remember that extremely elevated white blood cell counts (>100,000/μL) represent a medical emergency requiring immediate intervention to prevent complications such as brain infarction and hemorrhage. 3