scholarly journals Francisella philomiragia Bacteremia in a Patient with Acute Respiratory Insufficiency and Acute-on-Chronic Kidney Disease

2015 ◽  
Vol 53 (12) ◽  
pp. 3947-3950 ◽  
Author(s):  
Ryan F. Relich ◽  
Romney M. Humphries ◽  
H. Reid Mattison ◽  
Jessica E. Miles ◽  
Edward R. Simpson ◽  
...  

Francisella philomiragiais a very uncommon pathogen of humans. Diseases caused by it are protean and have been reported largely in near-drowning victims and those with chronic granulomatous disease. We present a case ofF. philomiragiapneumonia with peripheral edema and bacteremia in a renal transplant patient and review the diverse reports ofF. philomiragiainfections.

2015 ◽  
Vol 53 (3) ◽  
pp. 1034-1037 ◽  
Author(s):  
Caroline Piau ◽  
Mallorie Kerjouan ◽  
Marc Le Mouel ◽  
Solene Patrat-Delon ◽  
Pierre-Louis Henaux ◽  
...  

Here we report in a human, a renal transplant patient, the first disseminated infection withNocardia cerradoensis, isolated after a brain biopsy. Species identification was based on 16S rRNA,gyrB, andhsp65gene analyses. Antibiotic treatment was successful by combining carbapenems and aminoglycosides and then switching to oral trimethoprim-sulfamethoxazole.


2016 ◽  
Vol 60 (9) ◽  
pp. 5130-5134 ◽  
Author(s):  
Maria F. Mojica ◽  
Christopher P. Ouellette ◽  
Amy Leber ◽  
M. Brian Becknell ◽  
Monica I. Ardura ◽  
...  

ABSTRACTStenotrophomonas maltophiliais an emerging multidrug-resistant (MDR) opportunistic pathogen for which new antibiotic options are urgently needed. We report our clinical experience treating a 19-year-old renal transplant recipient who developed prolonged bacteremia due to metallo-β-lactamase-producingS. maltophiliarefractory to conventional treatment. The infection recurred despite a prolonged course of colistimethate sodium (colistin) but resolved with the use of a novel drug combination with clinical efficacy against the patient'sS. maltophiliaisolate.


2011 ◽  
Vol 55 (7) ◽  
pp. 3564-3566 ◽  
Author(s):  
Saskia Kuipers ◽  
Roger J. M. Brüggemann ◽  
Ruud G. L. de Sévaux ◽  
John P. F. A. Heesakkers ◽  
Willem J. G. Melchers ◽  
...  

ABSTRACTWe report the case of a kidney transplant recipient with invasive aspergillosis due toAspergillus fumigatusresistant to voriconazole and intermediately susceptible to posaconazole who failed posaconazole therapy. Plasma posaconazole concentrations indicated an unfavorable ratio of the area under the concentration-time curve over the MIC. Posaconazole should be used with caution for invasive aspergillosis caused by strains with attenuated posaconazole susceptibility, as drug exposure may be inadequate, resulting in therapeutic failure.


2019 ◽  
Vol 64 (1) ◽  
Author(s):  
Saskia Kuipers ◽  
Mike M. Ruth ◽  
Mike Mientjes ◽  
Ruud G. L. de Sévaux ◽  
Jakko van Ingen

ABSTRACT We report a case of a 58-year-old renal transplant patient who developed a recurrent urinary tract infection with an extended-spectrum β-lactamase (ESBL)-positive Klebsiella pneumoniae strain in the first month posttransplant. Even though it tested susceptible to carbapenems and despite repeated meropenem treatment, his infection recurred. The infection eventually evolved into epididymitis that was successfully treated with meropenem and bacteriophages. This case demonstrates the difficulty of treating relapsing ESBL-positive Gram-negative infections in renal transplant patients.


2017 ◽  
Vol 2017 ◽  
pp. 1-4
Author(s):  
Murtaza Mazhar ◽  
Ijlal Akbar Ali ◽  
Nelson Iván Agudelo Higuita

We present a case of a 71-year-old Vietnamese man with chronic kidney disease secondary to adult polycystic kidney disease. He had been a prisoner of war before undergoing a successful cadaveric renal transplant in the United States. He presented to clinic one year after the transplant with gross hematuria, productive cough, intermittent chills, and weight loss. Long standing peripheral eosinophilia of 600–1200/μL triggered further evaluation. A wet mount of stool revealedStrongyloides stercoralislarvae. A computed tomography (CT) of chest showed findings suggestive of extension of the infection to the lungs. The patient was treated with a three-week course of ivermectin with complete resolution of signs, symptoms, peripheral eosinophilia, and the positive IgG serology. Strongyloides infection in renal transplant patient is very rare and often presents with hyperinfection, associated with high mortality rates. The American Transplant Society recommends pretransplant screening with stool examination andStrongyloides stercoralisantibody in recipients and donors from endemic areas or with eosinophilia. It is imperative that healthcare professionals involved in the care of these individuals be cognizant of these recommendations as it is a very preventable and treatable entity.


1999 ◽  
Vol 5 (1) ◽  
pp. 67-69 ◽  
Author(s):  
Balázs Nemes ◽  
Hemangshu Podder ◽  
Jenő Járay ◽  
Gabriella Dabasi ◽  
Laura Lázár ◽  
...  

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