TY - JOUR
T1 - BK polyomavirus nephropathy after heart transplantation
T2 - A case report
AU - Iwasaki, Yoichi
AU - Seguchi, Osamu
AU - Ikura, Megumi
AU - Arisato, Tetsuya
AU - Hada, Tasuku
AU - Mochizuki, Hiroki
AU - Kuroda, Kensuke
AU - Nakajima, Seiko
AU - Watanabe, Takuya
AU - Tsukamoto, Yasumasa
AU - Yanase, Masanobu
AU - Yoshihara, Fumiki
AU - Ikeda, Yoshihiko
AU - Hatakeyama, Kinta
AU - Fukushima, Satsuki
AU - Fujita, Tomoyuki
AU - Fukushima, Norihide
N1 - Publisher Copyright:
© 2024
PY - 2024
Y1 - 2024
N2 - We present a case of BK polyomavirus (BKV) nephropathy (BKVN) after heart transplantation (HTx). The patient was a male with non-ischemic cardiomyopathy who received HTx at the age of 56 years [serum creatinine (sCre) at the time of HTx: 0.89 mg/dl]. Following 3 months of standard triple immunosuppression using tacrolimus, mycophenolate, and corticosteroid, everolimus with reduced tacrolimus therapy was introduced because of cardiac allograft vasculopathy. However, renal function gradually deteriorated. BKVN was diagnosed via positive simian virus 40 antigen staining of renal biopsy specimens 46 months after HTx (sCre: 2.48 mg/dl). Decoy cells and elevated serum BKV load were also observed. After reduction of immunosuppression and monthly low-dose intravenous immunoglobulin administration, the serum BKV load decreased and sCre plateaued while on uneventful clinical course. Since renal function is an important prognostic factor after HTx, early diagnosis and intervention are crucial for successful BKVN treatment. Urine cytology should be performed during post-transplant screening for renal dysfunction. Learning objective: BK polyomavirus nephropathy (BKVN) is a critical issue following solid organ transplantation. However, reports regarding BKVN after heart transplantation (HTx) are sparse, possibly underestimating the significance of BKVN in HTx recipients, therefore case studies are crucial for the understanding of BKVN in HTx recipients. This case clearly demonstrated the clinical course of BKVN and highlights the important clinical implications for the diagnosis and management of BKVN in HTx recipients.
AB - We present a case of BK polyomavirus (BKV) nephropathy (BKVN) after heart transplantation (HTx). The patient was a male with non-ischemic cardiomyopathy who received HTx at the age of 56 years [serum creatinine (sCre) at the time of HTx: 0.89 mg/dl]. Following 3 months of standard triple immunosuppression using tacrolimus, mycophenolate, and corticosteroid, everolimus with reduced tacrolimus therapy was introduced because of cardiac allograft vasculopathy. However, renal function gradually deteriorated. BKVN was diagnosed via positive simian virus 40 antigen staining of renal biopsy specimens 46 months after HTx (sCre: 2.48 mg/dl). Decoy cells and elevated serum BKV load were also observed. After reduction of immunosuppression and monthly low-dose intravenous immunoglobulin administration, the serum BKV load decreased and sCre plateaued while on uneventful clinical course. Since renal function is an important prognostic factor after HTx, early diagnosis and intervention are crucial for successful BKVN treatment. Urine cytology should be performed during post-transplant screening for renal dysfunction. Learning objective: BK polyomavirus nephropathy (BKVN) is a critical issue following solid organ transplantation. However, reports regarding BKVN after heart transplantation (HTx) are sparse, possibly underestimating the significance of BKVN in HTx recipients, therefore case studies are crucial for the understanding of BKVN in HTx recipients. This case clearly demonstrated the clinical course of BKVN and highlights the important clinical implications for the diagnosis and management of BKVN in HTx recipients.
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U2 - 10.1016/j.jccase.2024.06.008
DO - 10.1016/j.jccase.2024.06.008
M3 - Article
AN - SCOPUS:85198290686
SN - 1878-5409
JO - Journal of Cardiology Cases
JF - Journal of Cardiology Cases
ER -