Renal transplantation remains the preferred treatment for end-stage renal disease, offering superior survival and quality of life compared with long-term dialysis. As graft survival improves, the incidence of malignancies due to immunosuppressive drugs such as prostate cancer is rising in this population1. Prostate cancer in renal transplant recipients is generally not considered high risk or locally advanced at diagnosis, and it is associated with good control and low mortality rates during follow-up. Additionally, renal transplant recipients are at a considerable risk of death from other causes, e.g., cardiovascular disease, infections, etc.
Solid organ transplant recipients face a higher overall absolute risk of cancer (5-year cumulative incidence of 4.4%) compared to the general population. While certain malignancies, such as kidney and colorectal cancers, show significantly higher incidence rates in recipients over age 50, the 5-year cumulative incidence of prostate cancer remains similar to or even lower than that of the general population at recommended screening ages2.
Conversely, recent data indicate a 3-year cumulative incidence of prostate cancer reaching 1.74% in renal transplant recipients, approximately twofold higher than in age-matched controls in the general population3. This highlights that while prostate cancer is not disproportionately increased by transplantation, the aging transplant population still requires standardized screening and management.
Open radical prostatectomy has been successfully performed in renal transplant patients for many years. However, it might carry higher risks, including increased blood loss (usually 400–600 mL), longer hospital stays, more wound-related complications, and a greater need for retraction near the graft, which can threaten the ureter or the anastomosis4.
In contrast, RARP provides three-dimensional magnification, tremor filtration, and precise dissection, allowing better visualization and reduced manipulation of the graft structures5. Studies show that RARP is associated with lower estimated blood loss (often 100–200 mL), fewer major complications, shorter length of stay, and comparable or better functional recovery, while maintaining similar oncological outcomes6. Zeng et al. reported low graft injury rates and stable renal function after RARP, with overall complication rates of about 17% and infrequent major complications7.
While existing literature has established the general feasibility of RARP in renal transplant recipients and identified common technical modifications such as adjusted port placement and modified lymphadenectomy, the granular, step-by-step technical execution of these modifications in a complex clinical scenario remains underreported. This case report provides a detailed procedural guide for surgeons encountering this challenging anatomy for the first time. By illustrating these technical nuances in a real-world case with a right-sided iliac fossa transplant, concurrent anticoagulation, and multiple comorbidities, the case complements the existing aggregate literature with practical, actionable guidance for the safe replication of this procedure.
Case Presentation:
A 66-year-old man presented with biopsy-confirmed prostate adenocarcinoma (Gleason 3+4=7a). His medical history included end-stage renal disease secondary to IgA nephropathy, a first renal transplant in the left iliac fossa in 1990 (later explanted), and a second functioning transplant in the right iliac fossa in 2009. The patient is on everolimus 1 mg twice daily, tacrolimus 3 mg twice daily, and prednisone 5 mg once daily. Additional comorbidities were coronary artery disease with prior stent placement and atrial fibrillation managed with long-term apixaban. He reported lower urinary tract symptoms with a post-void residual volume of approximately 200 mL. He also complained about long-standing erectile dysfunction.
Diagnosis, Assessment, and Plan:
Physical examination showed good general condition with stable cardiopulmonary status. Digital rectal examination revealed a prostate of about 50 mL without nodules. Transrectal ultrasound confirmed a 49 mL prostate with homogeneous parenchyma and intact capsule; pelvic doppler ultrasound verified a well-perfused right iliac transplant. Laboratory findings included creatinine 1.25 mg/dL and eGFR 61 mL/min/1.73 m2.
After a multidisciplinary discussion involving urology, nephrology, and cardiology, the patient was deemed suitable for surgical treatment. The plan was nerve-sparing RARP with bilateral pelvic lymphadenectomy, chosen for its precision in altered anatomy and low risk profile. Potential complications discussed included transient renal impairment, lymphocele, and graft injury; anticoagulation was managed per institutional protocol.