BK virus-associated nephropathy in a lung transplant patient: case report and literature review.
BK Virus
/ genetics
DNA, Viral
/ metabolism
Humans
Immunoglobulins, Intravenous
/ therapeutic use
Immunosuppressive Agents
/ therapeutic use
Kidney Transplantation
Lung Transplantation
/ adverse effects
Male
Methylprednisolone
/ therapeutic use
Middle Aged
Mycophenolic Acid
/ therapeutic use
Polyomavirus Infections
/ diagnosis
Pulmonary Disease, Chronic Obstructive
/ therapy
Tumor Virus Infections
/ diagnosis
BK virus
Case report
End-stage renal failure
Lung transplantation
Nephropathy
Journal
BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551
Informations de publication
Date de publication:
14 Aug 2020
14 Aug 2020
Historique:
received:
01
04
2020
accepted:
26
07
2020
entrez:
16
8
2020
pubmed:
17
8
2020
medline:
9
9
2020
Statut:
epublish
Résumé
BK virus-associated nephropathy (BKVAN) is a relatively common cause of renal dysfunction in the first six months after renal transplantation. It arises from reactivation of the latent and usually harmless BK virus (BK virus) due to immunosuppression and other factors including some that are unique to renal transplantation such as allograft injury. BKVAN is much rarer in non-renal solid organ transplantation, where data regarding diagnosis and management are extremely limited. We report a case of a 58-year-old man found to have worsening renal dysfunction nine months after bilateral sequential lung transplantation for chronic obstructive pulmonary disease (COPD). He had required methylprednisolone for acute allograft rejection but achieved good graft function. Urine microscopy and culture and renal ultrasound were normal. BK virus PCR was positive at high levels in urine and blood. Renal biopsy subsequently confirmed BKVAN. The patient progressed to end-stage renal failure requiring haemodialysis despite reduction in immunosuppression, including switching mycophenolate for everolimus, and the administration of intravenous immunoglobulin (IVIG). This very rare case highlights the challenges presented by BK virus in the non-renal solid organ transplant population. Diagnosis can be difficult, especially given the heterogeneity with which BKV disease has been reported to present in such patients, and the optimal approach to management is unknown. Balancing reduction in immunosuppression against prevention of allograft rejection is delicate. Improved therapeutic options are clearly required.
Sections du résumé
BACKGROUND
BACKGROUND
BK virus-associated nephropathy (BKVAN) is a relatively common cause of renal dysfunction in the first six months after renal transplantation. It arises from reactivation of the latent and usually harmless BK virus (BK virus) due to immunosuppression and other factors including some that are unique to renal transplantation such as allograft injury. BKVAN is much rarer in non-renal solid organ transplantation, where data regarding diagnosis and management are extremely limited.
CASE PRESENTATION
METHODS
We report a case of a 58-year-old man found to have worsening renal dysfunction nine months after bilateral sequential lung transplantation for chronic obstructive pulmonary disease (COPD). He had required methylprednisolone for acute allograft rejection but achieved good graft function. Urine microscopy and culture and renal ultrasound were normal. BK virus PCR was positive at high levels in urine and blood. Renal biopsy subsequently confirmed BKVAN. The patient progressed to end-stage renal failure requiring haemodialysis despite reduction in immunosuppression, including switching mycophenolate for everolimus, and the administration of intravenous immunoglobulin (IVIG).
CONCLUSIONS
CONCLUSIONS
This very rare case highlights the challenges presented by BK virus in the non-renal solid organ transplant population. Diagnosis can be difficult, especially given the heterogeneity with which BKV disease has been reported to present in such patients, and the optimal approach to management is unknown. Balancing reduction in immunosuppression against prevention of allograft rejection is delicate. Improved therapeutic options are clearly required.
Identifiants
pubmed: 32795251
doi: 10.1186/s12879-020-05292-0
pii: 10.1186/s12879-020-05292-0
pmc: PMC7427921
doi:
Substances chimiques
DNA, Viral
0
Immunoglobulins, Intravenous
0
Immunosuppressive Agents
0
Mycophenolic Acid
HU9DX48N0T
Methylprednisolone
X4W7ZR7023
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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