Primary leiomyosarcoma of the seminal vesicle: case report and review of the literature

Primary leiomyosarcoma of the seminal vesicle is exceedingly rare. We report a case of a 59-year-old man with tumour detected by rectal symptoms and ultrasonography. Computed tomography and magnetic resonance imaging suggested an origin in the right seminal vesicle. Transperineal biopsy of the tumou...

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Veröffentlicht in:BMC cancer 2011-07, Vol.11 (1), p.323-323, Article 323
Hauptverfasser: Cauvin, Cécile, Moureau-Zabotto, Laurence, Chetaille, Bruno, Hilgers, Werner, Denoux, Yves, Jacquemier, Jocelyne, Guiramand, Jérôme, Sarran, Anthony, Bertucci, François
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Sprache:eng
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Zusammenfassung:Primary leiomyosarcoma of the seminal vesicle is exceedingly rare. We report a case of a 59-year-old man with tumour detected by rectal symptoms and ultrasonography. Computed tomography and magnetic resonance imaging suggested an origin in the right seminal vesicle. Transperineal biopsy of the tumour revealed leiomyosarcoma. A radical vesiculo-prostactectomy with bilateral pelvic lymphadenectomy was performed. Pathological examination showed a grade 2 leiomyosarcoma of the seminal vesicle. The patient received adjuvant radiotherapy. He developed distant metastases 29 months after diagnosis, and received chemotherapy. Metastatic disease was controlled by second-line gemcitabine-docetaxel combination. Fifty-one months after diagnosis of the primary tumour, and 22 months after the first metastases, the patient is alive with excellent performance status, and multiple asymptomatic stable lung and liver lesions. We report the eighth case of primary leiomyosarcoma of the seminal vesicle and the first one with a so long follow-up.
ISSN:1471-2407
1471-2407
DOI:10.1186/1471-2407-11-323