A 45‐yr‐old Japanese male underwent living‐related kidney transplantation in August 2005, and immunosuppression consisted of tacrolimus, mycophenolate mofetil, methylprednisolone, basiliximab, and rituximab 200 mg. Allograft function was good, and the protocol biopsy post‐transplant day 11 showed no evidence of rejection. The serum creatinine (s‐Cr) level was maintained at the 1.2 mg/dL for 18 months. On February 2007, the patient’s s‐Cr level had increased to 2.03 mg/dL, and an episode biopsy was performed. The biopsy specimen demonstrated moderate to severe tubulitis and moderate interstitial infiltration of plasma cells and lymphocytes. The inflammatory cell infiltrate consisted of >30% plasma cells. The histopathological findings were consistent with plasma cell‐rich acute rejection (PCAR). The PCAR was treated by steroid pulse therapy, and his s‐Cr level decreased to 1.58 mg/dL. A biopsy three months after the steroid pulse therapy showed no evidence of rejection. The patient’s allograft function is currently stable, and s‐Cr level is 1.7 mg/dL. This is a case of PACR, that was successfully treated with steroid pulse therapy alone.