1. Management of Males with 45,X/46,XY Gonadal Dysgenesis.
- Author
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Müller, Jørn, Ritzén, E. Martin, Ivarsson, Sten-A., Rajpert-De Meyts, Ewa, Norjavaara, Ensio, and Skakkebæk, Niels E.
- Subjects
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TURNER'S syndrome , *SEX chromosome abnormalities , *SEX differentiation disorders , *DISEASES in men , *CANCER in men , *HYPOSPADIAS , *CRYPTORCHISM - Abstract
Males with the 45,X/46,XY karyotype and malformations of the external genitalia carry an increased risk of developing germ cell neoplasia of the gonads. We have studied gonadal tissue from 10 individuals, 0.3–17 years of age, with a male phenotype and either hypospadias and/or cryptorchidism. Four patients, 0.3–15 years of age, had carcinoma in situ, 1 boy had Sertoli-cell-only pattern and the remainder prepubertal histology. Gonadoblastoma or invasive carcinoma was not found. On the basis of our current knowledge we propose a strategy for management and follow-up of these boys in order to detect possible premalignant histological changes early and prevent development of a gonadal tumour.Copyright © 2000 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]
- Published
- 1999
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