The management of Von Hippel-Lindau (VHL) disease is complex because of its autosomal dominant inheritance and propensity for the development of multiple, recurrent tumors across various organ systems1. A germline mutation in the VHL tumor suppressor gene leads to constitutive activation of hypoxia-inducible factors (HIFs), promoting angiogenesis and tumorigenesis2.
Clear cell renal cell carcinoma (ccRCC) is a leading cause of mortality in patients with VHL, with a lifetime risk of up to 70%3. A key principle in managing VHL-associated renal tumors is nephron-sparing surgery (NSS), which aims to preserve renal function and delay or prevent the need for dialysis4, particularly given the high likelihood of tumor recurrence and the potential need for future interventions.
The therapeutic landscape for VHL-associated ccRCC has recently expanded with the introduction of belzutifan, a HIF-2α inhibitor5. However, not all patients achieve a complete or sustained response, and disease progression during therapy may occur, necessitating surgical intervention5.
In relatively young patients with a solitary kidney, preservation of functional renal parenchyma is particularly important. In such cases, robotic-assisted partial nephrectomy (RAPN) offers the benefits of minimally invasive surgery and enhanced surgical precision, which may facilitate complex tumor resection and renorrhaphy6. A series of RAPN procedures in solitary kidneys demonstrated high rates of dialysis avoidance and successful preservation of estimated glomerular filtration rate (eGFR)7. However, these patients are inherently at increased risk of postoperative acute kidney injury (AKI)8. Severe AKI requiring renal replacement therapy (RRT), although less frequent, remains an important potential complication in this high-risk population.
This case report describes the perioperative management and outcomes of a patient with VHL disease and a solitary kidney who underwent RAPN for multifocal ccRCC that progressed despite belzutifan treatment. The case highlights the technical feasibility of nephron-sparing surgery and the significant challenge of postoperative AKI requiring intensive care and continuous RRT, underscoring the delicate balance between oncologic control and renal function preservation in this complex patient population.
Case presentation
A 37-year-old man with a confirmed diagnosis of Von Hippel-Lindau (VHL) disease was evaluated for multifocal renal tumors. Genetic testing performed in August 2024 identified a germline VHL mutation, c.257C > G (p.P86R). The patient was asymptomatic, and the tumors were suspected on surveillance imaging. The family history was positive for VHL.
The medical history was notable for multifocal clear cell renal cell carcinoma (ccRCC) of the left kidney. An open partial nephrectomy of the left kidney was initially performed at another hospital on November 13, 2024. Histopathological examination confirmed multifocal clear-cell RCC with a positive surgical margin at the lower pole (R1). Because of a postoperative urinoma associated with severe complications, radical left nephrectomy was subsequently performed on December 27, 2024.
On May 1, 2025, treatment with belzutifan at 120 mg daily was initiated as systemic therapy for VHL-associated tumors. Despite treatment, surveillance imaging in October 2025 demonstrated progression of three pre-existing ccRCC lesions in the solitary right kidney (Table 1). The largest lesion, located in the mid-kidney, measured approximately 4.8 cm, compared with 3.1 cm in October 2024, and was in close contact with the renal collecting system. Two additional lesions, measuring approximately 2–2.5 cm, were identified at the upper pole (Figure 1 and Figure 2). Preoperative laboratory values were stable, with a serum creatinine level of 1.2 mg/dL and an estimated glomerular filtration rate (eGFR) of 83 mL/min/1.73 m2 (Table 1). The patient strongly preferred a minimally invasive, nephron-sparing procedure and declined open or radical surgical approaches.
Postoperative laboratory course
Following surgery, acute kidney injury with anuria developed. Serial laboratory assessments demonstrated progressive renal impairment, with serum creatinine reaching a peak of 4.8 mg/dL on postoperative day (POD) 3.
Diagnosis, assessment, and plan
Progressive multifocal ccRCC in a solitary kidney was diagnosed based on imaging findings and the established history of VHL disease. Extensive preoperative planning was undertaken. High-resolution abdominal MRI was performed to delineate the anatomical relationships among the tumors, renal vasculature, and collecting system (Figure 1 and Figure 2). This facilitated detailed preoperative mapping and planning of a sequential tumor resection strategy.
The primary surgical objective was complete tumor excision with negative surgical margins while minimizing warm ischemia time and preserving maximal renal function in the solitary kidney. Given the complex anatomy and preference for a minimally invasive nephron-sparing approach, transperitoneal robotic-assisted partial nephrectomy (RAPN) was selected. The surgical strategy involved sequential tumor resection, beginning with the most complex mid-kidney lesion.