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Published on: July 19, 2024
Two cases of q-Fever in hairy cell leukemia
Emanuele Ammatuna1, Emilio Iannitto2, Lidwine W Tick3
1Department of Hematology, Erasmus University Medical Centre, Daniel den Hoed, Groene Hilledijk 301, 3075 EA Rotterdam, The Netherlands.
Insights
This study highlights Q-fever as an initial symptom in two hairy cell leukemia (HCL) patients. Prompt HCL treatment with cladribine achieved remission, emphasizing vigilance for Q-fever in HCL patients.
Area of Science:
- Hematology
- Infectious Diseases
- Oncology
Background:
- Hairy cell leukemia (HCL) is a rare B-cell neoplasm.
- HCL patients exhibit significant susceptibility to infections.
- Q-fever, caused by Coxiella burnetii (CB), is an infection that can present unusually in immunocompromised individuals.
Purpose of the Study:
- To report two cases of Q-fever presenting as the initial manifestation in patients with HCL.
- To discuss the clinical course, treatment challenges, and outcomes of these patients.
- To raise awareness of Q-fever as a potential presenting infection in HCL.
Main Methods:
- Case report of two patients diagnosed with HCL.
- Description of clinical presentation, diagnostic workup, and treatment protocols for both Q-fever and HCL.
- Analysis of treatment response and patient outcomes.
Main Results:
- Two HCL patients presented with Q-fever as their first disease manifestation.
- Patients showed a slow response to ciprofloxacin for Q-fever, likely due to immunodeficiency.
- Successful HCL treatment with cladribine post-Q-fever resolution resulted in complete remission.
Conclusions:
- Q-fever should be considered in febrile HCL patients, particularly in endemic areas.
- The potential for chronic infection in HCL patients warrants attention.
- Further case reporting is encouraged to better understand the association between CB infection and HCL.
Abstract:
Hairy cell leukemia (HCL) is a rare B-cell lymphoproliferative disorder accounting for about 2% of all leukemias. The clinical course is indolent, however HCL patients are particularly susceptible to infections. Here we report two cases of Q-fever as first manifestation of disease in two patients affected by HCL. Both patients described in this report showed an unusually sluggish clinical response to the antibiotic treatment with ciprofloxacin probably because of the marked immunodeficiency. However, treatment of HCL with cladribine administered soon after the resolution of QF pneumonitis was uneventful and led to a complete remission in both cases. Most probably the association of Coxiella burnetii (CB) infection and HCL that we observed in two patients is due to chance. However, a hairy cell resembling transformation of freshly isolated human peripheral blood lymphocytes upon CB has been showed. We think that the possibility of CB infection in febrile HCL patient should be always taken in mind, especially in endemic areas. In addition the potential for such infections to become chronic in HCL patients should not be overlooked and the reporting of further cases should be encouraged.
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