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.

Case Reports in Hematology
|September 3, 2014
PubMed

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.

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