Abstract:Background: There is a growing base of literature describing BK nephropathy (BKVN) in patients outside of the setting of kidney transplant. Previous systematic reviews of the literature have been limited by methodology or by the scope of patients included.
Study Design and Methods:Systematic Review (Prospero # CRD42018088524).
Setting & Population:Patients without kidney transplant who had biopsy-proven BKVN.
Selection Criteria for Studies:Full-text articles that describe native BKVN patient cases.Analytica… Show more
“…Approximately, 80% of RT recipients develop BK viruria, and 5%‐10% of these patients develop BKVN within a year post‐RT with allograft loss in about 50% 2 . However, several reports of native kidney BK nephropathy in both adult and pediatric non‐RT patients have been described in the recent literature 3 . This includes patients with HSCT, non‐renal SOT, HIV, hematological malignancies, and other immunodeficiency conditions 4,5 .…”
BK virus encephalitis after HSCT is uncommon. Several reports of native kidney BKVN in patients with HSCT, hematologic malignancies, human immunodeficiency virus infection, and non‐renal solid organ transplantation have been described. However, an uncommon combination of BK encephalitis and ESRD of native kidneys secondary to BK virus in a child with HSCT has not been described. We report a 10‐year‐old boy who presented with a gradually rising serum creatinine during treatment for severe autoimmune hemolytic anemia, which he developed 9 months after receiving an allogeneic HSCT for aplastic anemia. There was no proteinuria or hematuria present. Serum BK virus load was 5 × 106 copies/mL. A renal biopsy showed evidence of BKVN. He developed fever, seizures, and confusion, and the (CSF) showed significant presence of the BK virus (1 × 106 copies/mL) along with biochemical evidence of viral encephalitis. Cerebrospinal fluid cultures were negative. Despite significant clinical symptoms and presence of BK virus in CSF, the magnetic resonance brain imaging findings were minimal. With reduction of immunosuppression, there was resolution of BK encephalitis but BKVN remained resistant to multiple anti‐BK virus agents, including leflunomide and cidofovir. He eventually became dialysis‐dependent and, 6 years later, received a renal transplant from his mother. This case illustrates that BK virus in severely immunocompromised HSCT recipient may lead to BK encephalitis and BKVN of native kidneys, even without hemorrhagic cystitis, leading to ESRD. Knowledge of such is important for appropriate timely evaluation and management.
“…Approximately, 80% of RT recipients develop BK viruria, and 5%‐10% of these patients develop BKVN within a year post‐RT with allograft loss in about 50% 2 . However, several reports of native kidney BK nephropathy in both adult and pediatric non‐RT patients have been described in the recent literature 3 . This includes patients with HSCT, non‐renal SOT, HIV, hematological malignancies, and other immunodeficiency conditions 4,5 .…”
BK virus encephalitis after HSCT is uncommon. Several reports of native kidney BKVN in patients with HSCT, hematologic malignancies, human immunodeficiency virus infection, and non‐renal solid organ transplantation have been described. However, an uncommon combination of BK encephalitis and ESRD of native kidneys secondary to BK virus in a child with HSCT has not been described. We report a 10‐year‐old boy who presented with a gradually rising serum creatinine during treatment for severe autoimmune hemolytic anemia, which he developed 9 months after receiving an allogeneic HSCT for aplastic anemia. There was no proteinuria or hematuria present. Serum BK virus load was 5 × 106 copies/mL. A renal biopsy showed evidence of BKVN. He developed fever, seizures, and confusion, and the (CSF) showed significant presence of the BK virus (1 × 106 copies/mL) along with biochemical evidence of viral encephalitis. Cerebrospinal fluid cultures were negative. Despite significant clinical symptoms and presence of BK virus in CSF, the magnetic resonance brain imaging findings were minimal. With reduction of immunosuppression, there was resolution of BK encephalitis but BKVN remained resistant to multiple anti‐BK virus agents, including leflunomide and cidofovir. He eventually became dialysis‐dependent and, 6 years later, received a renal transplant from his mother. This case illustrates that BK virus in severely immunocompromised HSCT recipient may lead to BK encephalitis and BKVN of native kidneys, even without hemorrhagic cystitis, leading to ESRD. Knowledge of such is important for appropriate timely evaluation and management.
“…In a recent review of the literature by Shah et al, biopsy-proven BKVN developing in the setting of solid organ transplantation accounted for approximately one third of all cases occurring in the native kidney. 5 With respect to BKVN in the native kidney, review of the literature reveals 3 liver (including the case reported herein), 13 heart, 6 lung, and 1 pancreas transplant recipients. Cases are described in both pediatric and adult populations, men and women, affect differing races, with variable combinations of immunosuppression, and with antiviral management strategies.…”
Section: Discussionmentioning
confidence: 84%
“…heart, lung, liver), hematologic malignancy (variably with bone marrow transplantation), and autoimmune disease. 4,5 Biopsy-proven BKVN in liver transplant recipients has been described sparingly. Lai et al described a 59-year-old male who was 2 years status post liver transplantation and presented acutely with biopsy-proven cytomegalovirus colitis, acute kidney injury (serum creatinine of 280 µmol/L), biopsy-proven BKVN, and 754,976 copies/mL of BK-virus in the serum.…”
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“…Native kidney BKV associated disease in non‐renal solid organ transplant (NRSOT) recipients has been described in case reports and series over the years, but it has not been systematically studied 12‐35 . BKV nephropathy in the NRSOT recipient has the potential to lead to chronic kidney disease (CKD) or end‐stage renal disease (ESRD) with associated morbidity and mortality 36‐38 .…”
We retrospectively examined the clinical characteristics, pathological features, and outcomes of BK viremia and nephropathy in a population of non‐renal solid organ transplant patients (NRSOT) referred for outpatient nephrology consultation over a period of 5 years. In the entire cohort of liver, heart, and lung transplant recipients referred to this clinic, 14% percent were found to have BK viremia with a median peak serum BK viral load of 35 500 copies/ml (range 250 to 21 100 000 copies/ml). BK viremia resolved in six of the seventeen patients (35%). Four out of five patients biopsied showed BK virus (BKV) nephropathy. Eleven out of seventeen patients with BK viremia developed advanced (stage 4 or 5) chronic kidney disease. Four patients developed rejection of their solid organ transplant within the first year post detection of BK viremia after immunosuppression reduction. We conclude that a multi‐center study is required to evaluate whether implementation of a systematic BK screening program would be effective in early detection and management of this problem in the NRSOT population.
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