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Published on: August 13, 2019
An unusual case of post-menopausal bleeding.
Roli Purwar1, Jyothi Kanugonda1, Mridula Shukla2
1Department of Surgical Oncology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
This case report highlights an extremely rare instance of vaginal metastasis from renal cell carcinoma (RCC) presenting as post-menopausal bleeding. Early detection and thorough investigation are crucial for managing this uncommon presentation of advanced RCC.
Area of Science:
- Oncology
- Urology
Background:
- Renal cell carcinoma (RCC) metastasis at presentation is common, typically affecting the lungs, bone, and liver.
- Synchronous vaginal and cervical metastasis from RCC is exceptionally rare, with blood reflux from the left renal vein to the ovarian vein being a proposed pathway.
- Metastatic tumors to the vagina are more frequently secondary to gynecological cancers (cervix, endometrium, ovary) than primary vaginal tumors.
Purpose of the Study:
- To report an extremely rare case of vaginal metastasis from renal cell carcinoma presenting as post-menopausal bleeding.
- To emphasize the importance of a high index of suspicion for diagnosing rare metastatic patterns of RCC.
- To discuss the diagnostic and management considerations for vaginal metastasis of renal origin.
Main Methods:
- A case presentation of a 55-year-old woman with post-menopausal bleeding.
- Physical examination revealed a vaginal mass obscuring the cervix.
- Diagnosis was confirmed via biopsy and immunohistochemistry, identifying renal cell carcinoma metastasis. Imaging identified a primary left renal mass and further metastases.
Main Results:
- The patient presented with a vaginal mass and confirmed vaginal, cervical, and pulmonary metastases from a left renal mass.
- Histopathological examination confirmed metastatic renal cell carcinoma.
- The patient was initiated on Pazopanib treatment.
Conclusions:
- Vaginal metastasis presenting as post-menopausal bleeding is an exceedingly rare manifestation of renal cell carcinoma, with only three prior cases reported.
- A high index of suspicion, thorough examination, and comprehensive investigation are critical for the accurate diagnosis and management of such rare presentations.
- While secondary vaginal tumors are more common, this case underscores the possibility of RCC as a source, necessitating a broad differential diagnosis.
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