2016
DOI: 10.1111/tid.12586
|View full text |Cite
|
Sign up to set email alerts
|

Fulminant Epstein–Barr virus‐associated hemophagocytic syndrome in a renal transplant patient and review of the literature

Abstract: We describe a rare fulminant case of Epstein-Barr virus-associated hemophagocytic syndrome (HPS) in a 37-year-old female renal transplant patient, indistinguishable from severe sepsis clinically and in the laboratory. HPS involves rapidly escalating immune system activation, resulting in a cytokine cascade, which can, especially in immunocompromised patients, lead to multi-organ failure, and even death. Thirty-two Herpesviridae-associated HPS cases in renal transplant patients have been reported and are review… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
4
0

Year Published

2017
2017
2022
2022

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(4 citation statements)
references
References 28 publications
0
4
0
Order By: Relevance
“…For the first time, we report a case of a rapid clinical recovery following rituximab and dexamethasone in a critically ill kidney transplant patient with likely COVID-19-driven EBV reactivation and features of secondary HLH. Secondary HLH is a rare but well-established complication of renal transplantation, triggered mostly by infections (in particular, viral such as EBV or CMV) or malignancy [ 1 ]. This life-threatening hyper-inflammatory condition is characterised by fever, (hepato) splenomegaly and cytopenias due to unregulated activation of cytotoxic T cells, NK cells and macrophages.…”
Section: Discussionmentioning
confidence: 99%
“…For the first time, we report a case of a rapid clinical recovery following rituximab and dexamethasone in a critically ill kidney transplant patient with likely COVID-19-driven EBV reactivation and features of secondary HLH. Secondary HLH is a rare but well-established complication of renal transplantation, triggered mostly by infections (in particular, viral such as EBV or CMV) or malignancy [ 1 ]. This life-threatening hyper-inflammatory condition is characterised by fever, (hepato) splenomegaly and cytopenias due to unregulated activation of cytotoxic T cells, NK cells and macrophages.…”
Section: Discussionmentioning
confidence: 99%
“…Since 1979, 21 cases of CMV-associated HLH in kidney transplant recipients were reported in the literature [8]. In the majority of cases, HLH occurred within 1 and 6 months after transplantation, and it represented a reactivation of a latent disease.…”
Section: Discussionmentioning
confidence: 99%
“…In the majority of cases, HLH occurred within 1 and 6 months after transplantation, and it represented a reactivation of a latent disease. Mortality was reported in 9 out of 21 cases (42.8%) [8]. For cases with an available detailed medical history, progression to lethal outcome was quite rapid, ranging from 9 to 21 days.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, rhabdomyolysis is recurrently associated with EBV-induced AKI and should be identified in these situations [ 171 ]. Hemophagocytic syndrome is a rare but dramatic complication of EBV infection caused by a cytokine storm that can lead to severe AKI [ 172 , 173 ]. Finally, some cases of glomerulonephritis and thrombotic microangiopathy have also been reported in the setting of primary EBV infection [ 171 , 174 , 175 ].…”
Section: The Herpesviridae Familymentioning
confidence: 99%