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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
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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)
CRYPTORCHIDISM
ORCHIOPEXY
FOLLOW-UP
GERM-CELL TUMOR
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