Gewählte Publikation:
MAYR, J; BREINL, E; RATSCHEK, M; HECHTL, W.
INVASIVE GERM-CELL TUMOR-DETECTED BY FOLLOW-UP EXAMINATION FOLLOWING ORCHIOPEXY FOR CRYPTORCHIDISM
PEDIAT SURG INT. 1995; 10(5-6): 427-429.
Doi: 10.1007/BF00182250
Web of Science
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- Abstract:
- The authors report the case of a 26-year-old man who was operated upon for bilateral testicular maldescent when he was 11 years old. In a follow-up examination for men with a history of orchiopexy for cryptorchidism, he palpated a dense nodule emerging from his right testis, and therapy for invasive testicular cancer was started. The histologic diagnosis was a mixed teratoma consisting of yolk-sac tumor, differentiated teratoma, and embryonic carcinoma. We conclude that young men with a history of testicular maldescent should be followed up by a multidisciplinary approach and should be offered testicular biopsy after puberty to allow detection and treatment of testicular intraepithelial neoplasia (so-called testicular carcinoma in situ) to prevent invasive testicular cancer.
- Find related publications in this database (Keywords)
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CRYPTORCHIDISM
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ORCHIOPEXY
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FOLLOW-UP
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GERM-CELL TUMOR