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Solitary penile neurofibroma with erectile dysfunction
Young Hwan Ji1, Sang Hyeon Cheon, Joong Ho Lee
1Department of Urology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.
Korean Journal of Urology
|July 14, 2011
Summary
A rare penile neurofibroma, a benign nerve tumor, caused sexual dysfunction in a 37-year-old man. Surgical removal resolved his symptoms and showed no signs of recurrence after 26 months.
Area of Science:
- Urology
- Oncology
- Dermatology
Background:
- Penile neurofibromas are rare tumors, often linked to neurofibromatosis type 1.
- Primary solitary neurofibromas of the penis are exceptionally uncommon.
Purpose of the Study:
- To report a case of a solitary neurofibroma of the penis.
- To discuss the clinical presentation and surgical management of this rare condition.
Main Methods:
- Case presentation of a 37-year-old male with a penile mass.
- Surgical excision of the neurofibroma.
- Post-operative follow-up for 26 months.
Main Results:
- The patient presented with a penile mass causing sexual intercourse difficulties and erectile dysfunction.
- Complete surgical excision of the neurofibroma was performed.
- Post-surgery, the patient experienced pain relief, normal penile glans sensation, and improved erectile function.
- No tumor recurrence was observed at 26 months follow-up.
Conclusions:
- Solitary penile neurofibromas, though rare, can cause significant functional impairment.
- Surgical excision is an effective treatment, leading to symptom resolution and no recurrence in this case.
- This case highlights the importance of considering rare penile tumors in the differential diagnosis.
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