Isolated clival metastasis: a rare presentation of renal cell carcinoma

Anil Mani1, Priyank Yadav1, Vimal Kumar Paliwal2

  • 1Department of Urology and Renal Transplant, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.

BMJ Case Reports
|August 13, 2017
PubMed

Insights

This case report highlights a rare instance of renal cell carcinoma metastasis presenting as a clival lesion causing headache and double vision. It underscores the importance of considering kidney cancer in patients with unexplained cranial nerve deficits.

Area of Science:

  • Oncology
  • Neurology
  • Radiology

Background:

  • Renal cell carcinoma (RCC) is a significant cause of adult malignancies, typically metastasizing to common sites like lymph nodes, lungs, bone, liver, and brain.
  • Clival tumors can present with diverse symptoms, including cranial neuropathies, often necessitating a thorough diagnostic workup.
  • Metastatic disease from renal primaries to the skull base is uncommon, making early diagnosis challenging.

Observation:

  • A patient presented with holocranial headache and diplopia, indicative of potential neurological compromise.
  • Cranial magnetic resonance imaging (MRI) revealed a clival-based lesion with associated bony erosion.
  • Abdominal ultrasonography and contrast-enhanced computed tomography (CT) identified a left renal mass, suggesting a primary renal tumor.

Findings:

  • The clival lesion was confirmed to be a metastasis from an otherwise occult renal cell carcinoma.
  • The absence of other metastatic foci emphasized the unusual presentation of this advanced malignancy.
  • The patient received radiotherapy for symptomatic management of the clival metastasis.

Implications:

  • This case emphasizes the critical need to evaluate clival lesions presenting with cranial neuropathies for a potential renal primary tumor.
  • It suggests that clinicians should maintain a high index of suspicion for uncommon metastatic patterns of renal cell carcinoma.
  • Prompt diagnosis and management of such rare presentations can potentially improve patient outcomes and guide further therapeutic strategies.