Literature DB >> 10640893

Management of males with 45,X/46,XY gonadal dysgenesis.

J Müller1, E M Ritzén, S A Ivarsson, E Rajpert-De Meyts, E Norjavaara, N E Skakkebaek.   

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

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Mesh:

Year:  1999        PMID: 10640893     DOI: 10.1159/000023425

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  6 in total

1.  Feminising surgery in male pseudohermaphrodites.

Authors:  Indre Zaparackaite; Vidmantas Barauskas; Ole Henrik Nielsen
Journal:  Pediatr Surg Int       Date:  2004-06-18       Impact factor: 1.827

2.  Synchronous bilateral breast carcinoma in a 50-year-old man with 45,X/46,XY mosaic karyotype: report of a case.

Authors:  Gianluca Franceschini; Pierfrancesco D'Alba; Melania Costantini; Andrea Magistrelli; Paolo Belli; Antonino Mulè; Claudio Coco; Aurelio Picciocchi
Journal:  Surg Today       Date:  2006       Impact factor: 2.549

3.  Intratubular germ cell neoplasia in a man with ambiguous genitalia, 45,X/46,XY mosaic karyotype, and Y chromosome microdeletions.

Authors:  Athanasios D Papanikolaou; Dimitrios G Goulis; Chariklia Giannouli; Christina Gounioti; John N Bontis; John Papadimas
Journal:  Endocr Pathol       Date:  2003       Impact factor: 3.943

4.  Short stature in children with an apparently normal male phenotype can be caused by 45,X/46,XY mosaicism and is susceptible to growth hormone treatment.

Authors:  Annette Richter-Unruh; Sabine Knauer-Fischer; Stefan Kaspers; Beate Albrecht; Gabriele Gillessen-Kaesbach; Berthold P Hauffa
Journal:  Eur J Pediatr       Date:  2004-02-18       Impact factor: 3.183

5.  Clinical and gonadal features and early surgical management of 45,X/46,XY and 45,X/47,XYY chromosomal mosaicism presenting with genital anomalies.

Authors:  M K Farrugia; N J Sebire; J C Achermann; A Eisawi; P G Duffy; I Mushtaq
Journal:  J Pediatr Urol       Date:  2012-01-26       Impact factor: 1.830

6.  A 45,X/46,XY Male with Orchidopexy Diagnosed with Mixed Germ Cell Tumor After 21-year Follow-up.

Authors:  Masashi Kubota; Naoki Terada; Katsuhiro Ito; Hideaki Takada; Toshihiro Magaribuchi; Atsuro Sawada; Shusuke Akamatsu; Hiromitsu Negoro; Ryoichi Saito; Takashi Kobayashi; Toshinari Yamasaki; Takahiro Inoue; Osamu Ogawa
Journal:  Urol Case Rep       Date:  2017-05-05
  6 in total

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