2020
DOI: 10.1111/tid.13441
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Very late‐onset cytomegalovirus disease with ganciclovir resistance >15 years following renal transplantation

Abstract: Cytomegalovirus (CMV) infection is a significant cause of morbidity and mortality after solid organ transplantation. There has been a significant shift in disease epidemiology with the introduction of antiviral prophylaxis, with CMV disease occurring later and clinical presentations more atypical. We describe two cases of very late‐onset CMV disease where first disease occurred 15 and 18 years post–renal transplantation, with both cases complicated by antiviral drug resistance. We subsequently review the publi… Show more

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Cited by 5 publications
(3 citation statements)
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“…Other factors such as immunosenescence associated with chronic kidney disease, postulated to be important in very late CMV disease, may have contributed. [13][14][15] In CDI, Clostridium difficile toxin disrupts cell signaling pathways, causing cell death and disruption of epithelial tight junctions, allowing the influx of neutrophils into the mucosa and formation of pseudomembranes. 16,17 The mechanism of pseudomembrane formation in CMV colitis may be similar to that in ischemic colitis.…”
Section: Discussionmentioning
confidence: 99%
“…Other factors such as immunosenescence associated with chronic kidney disease, postulated to be important in very late CMV disease, may have contributed. [13][14][15] In CDI, Clostridium difficile toxin disrupts cell signaling pathways, causing cell death and disruption of epithelial tight junctions, allowing the influx of neutrophils into the mucosa and formation of pseudomembranes. 16,17 The mechanism of pseudomembrane formation in CMV colitis may be similar to that in ischemic colitis.…”
Section: Discussionmentioning
confidence: 99%
“…Сравнительный анализ одногодичной выживаемости без нежелательных событий (летальность, отторжение, возврат на гемодиализ) у реципиентов почки в зависимости от стратегии профилактики ЦМВ-инфекции не показал статистических различий (р = 0,537). угольными камнями профилактики ЦМВ-инфекции, однако их недостаточно для предотвращения репликации вируса [11]. За последние два десятилетия стало ясно, что как врожденный, так и специфический иммунитет имеют большое значение в контроле ЦМВ, что потребовало оптимизации протоколов иммуносупрессивной терапии.…”
Section: оценка нежелательных иммунологических событийunclassified
“…CMV infection is defined as the presence of CMV replication in tissue, blood, or other bodily fluids regardless of symptomatology, while CMV disease requires CMV infection that is accompanied by clinical signs and symptoms 2 . When CMV disease happens after completion of antiviral prophylaxis it is denominated delayed-onset CMV disease, and when it occurs more than 12 months after transplantation, it is classified as late onset 3 .…”
Section: Introductionmentioning
confidence: 99%