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Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature
BACKGROUND: Helicobacter cinaedi is a rare pathogen in humans, occurring mostly in immuno-compromised patients, with a high potential for recurrence. We describe a case of a patient with lymphoma hospitalized for chemotherapy. CASE PRESENTATION: At admission, the patient presented with an indolent a...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1482711/ https://www.ncbi.nlm.nih.gov/pubmed/16719920 http://dx.doi.org/10.1186/1471-2334-6-86 |
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author | Uçkay, Ilker Garbino, Jorge Dietrich, Pierre-Yves Ninet, Béatrice Rohner, Peter Jacomo, Véronique |
author_facet | Uçkay, Ilker Garbino, Jorge Dietrich, Pierre-Yves Ninet, Béatrice Rohner, Peter Jacomo, Véronique |
author_sort | Uçkay, Ilker |
collection | PubMed |
description | BACKGROUND: Helicobacter cinaedi is a rare pathogen in humans, occurring mostly in immuno-compromised patients, with a high potential for recurrence. We describe a case of a patient with lymphoma hospitalized for chemotherapy. CASE PRESENTATION: At admission, the patient presented with an indolent and non-prurigenic macular rash around her implantable venous access device. Gram staining of blood cultures revealed the presence of spiral-shaped gram-negative rods that could not be grown upon subculture. Helicobacter cinaedi was identified by PCR. No other symptoms or pathology were observed in a whole body CT scan. The implantable venous access device was removed and empiric therapy by ceftriaxone and gentamicin for 2 weeks was initiated, followed by peroral clarithromycin 2 × 500 mg/day and later by levofloxacin 2 × 500 mg/day for 7 weeks. Oncologic remission was achieved 3 months later. However, the patient was re-hospitalized 2 months later for fever, shivering, reappearance of the macular non-prurigenic rash, diarrhea, cough and asthenia. Blood cultures grew H. cinaedi. Multiple investigations could not identify the source. Empiric antibiotic therapy of ceftriaxone and doxycycline was started for 2 weeks with resolution of symptoms, followed by an oral combination of amoxicillin, metronidazole and doxycycline for 2 months; doxycycline was continued for another month. Bacteremia has not recurred for a period of 19 months. CONCLUSION: Although H. cinaedi is considered to be a low virulent bacteria, its potential to cause recurrent bacteremia should not be underestimated. H. cinaedi could have an endovascular source of infection and should be treated for an adequate duration with combined antibiotherapy. |
format | Text |
id | pubmed-1482711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-14827112006-06-24 Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature Uçkay, Ilker Garbino, Jorge Dietrich, Pierre-Yves Ninet, Béatrice Rohner, Peter Jacomo, Véronique BMC Infect Dis Case Report BACKGROUND: Helicobacter cinaedi is a rare pathogen in humans, occurring mostly in immuno-compromised patients, with a high potential for recurrence. We describe a case of a patient with lymphoma hospitalized for chemotherapy. CASE PRESENTATION: At admission, the patient presented with an indolent and non-prurigenic macular rash around her implantable venous access device. Gram staining of blood cultures revealed the presence of spiral-shaped gram-negative rods that could not be grown upon subculture. Helicobacter cinaedi was identified by PCR. No other symptoms or pathology were observed in a whole body CT scan. The implantable venous access device was removed and empiric therapy by ceftriaxone and gentamicin for 2 weeks was initiated, followed by peroral clarithromycin 2 × 500 mg/day and later by levofloxacin 2 × 500 mg/day for 7 weeks. Oncologic remission was achieved 3 months later. However, the patient was re-hospitalized 2 months later for fever, shivering, reappearance of the macular non-prurigenic rash, diarrhea, cough and asthenia. Blood cultures grew H. cinaedi. Multiple investigations could not identify the source. Empiric antibiotic therapy of ceftriaxone and doxycycline was started for 2 weeks with resolution of symptoms, followed by an oral combination of amoxicillin, metronidazole and doxycycline for 2 months; doxycycline was continued for another month. Bacteremia has not recurred for a period of 19 months. CONCLUSION: Although H. cinaedi is considered to be a low virulent bacteria, its potential to cause recurrent bacteremia should not be underestimated. H. cinaedi could have an endovascular source of infection and should be treated for an adequate duration with combined antibiotherapy. BioMed Central 2006-05-23 /pmc/articles/PMC1482711/ /pubmed/16719920 http://dx.doi.org/10.1186/1471-2334-6-86 Text en Copyright © 2006 Uçkay et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Uçkay, Ilker Garbino, Jorge Dietrich, Pierre-Yves Ninet, Béatrice Rohner, Peter Jacomo, Véronique Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature |
title | Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature |
title_full | Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature |
title_fullStr | Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature |
title_full_unstemmed | Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature |
title_short | Recurrent bacteremia with Helicobacter cinaedi: case report and review of the literature |
title_sort | recurrent bacteremia with helicobacter cinaedi: case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1482711/ https://www.ncbi.nlm.nih.gov/pubmed/16719920 http://dx.doi.org/10.1186/1471-2334-6-86 |
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