Two Cases of Q-Fever in Hairy Cell Leukemia

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 af...

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Main Authors: Emanuele Ammatuna, Emilio Iannitto, Lidwine W. Tick, Nicolaas L. A. Arents, Philip H. Kuijper, Marten R. Nijziel
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2014/863932
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spelling doaj-b4b546a70cae46b2bddfb9fd3b0beac02020-11-25T01:10:25ZengHindawi LimitedCase Reports in Hematology2090-65602090-65792014-01-01201410.1155/2014/863932863932Two Cases of Q-Fever in Hairy Cell LeukemiaEmanuele Ammatuna0Emilio Iannitto1Lidwine W. Tick2Nicolaas L. A. Arents3Philip H. Kuijper4Marten R. Nijziel5Department of Hematology, Erasmus University Medical Centre, Daniel den Hoed, Groene Hilledijk 301, 3075 EA Rotterdam, The NetherlandsDepartment of Oncology, Haematology Unit, University of Palermo School of Medicine, Palermo, ItalyDepartment of Internal Medicine, Maxima Medical Centre, The NetherlandsLaboratory for Medical Microbiology, PAMM Foundation, Veldhoven, The NetherlandsDepartment of Clinical Chemistry, Máxima Medical Centre, Veldhoven, The NetherlandsDepartment of Internal Medicine, Maxima Medical Centre, The NetherlandsHairy 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.http://dx.doi.org/10.1155/2014/863932
collection DOAJ
language English
format Article
sources DOAJ
author Emanuele Ammatuna
Emilio Iannitto
Lidwine W. Tick
Nicolaas L. A. Arents
Philip H. Kuijper
Marten R. Nijziel
spellingShingle Emanuele Ammatuna
Emilio Iannitto
Lidwine W. Tick
Nicolaas L. A. Arents
Philip H. Kuijper
Marten R. Nijziel
Two Cases of Q-Fever in Hairy Cell Leukemia
Case Reports in Hematology
author_facet Emanuele Ammatuna
Emilio Iannitto
Lidwine W. Tick
Nicolaas L. A. Arents
Philip H. Kuijper
Marten R. Nijziel
author_sort Emanuele Ammatuna
title Two Cases of Q-Fever in Hairy Cell Leukemia
title_short Two Cases of Q-Fever in Hairy Cell Leukemia
title_full Two Cases of Q-Fever in Hairy Cell Leukemia
title_fullStr Two Cases of Q-Fever in Hairy Cell Leukemia
title_full_unstemmed Two Cases of Q-Fever in Hairy Cell Leukemia
title_sort two cases of q-fever in hairy cell leukemia
publisher Hindawi Limited
series Case Reports in Hematology
issn 2090-6560
2090-6579
publishDate 2014-01-01
description 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.
url http://dx.doi.org/10.1155/2014/863932
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