Risk of gonadal neoplasia in patients with disorders/differences of sex development

•Patients with DSD and the Y chromosome have the highest risk of gonadal germ cell neoplasia.•Particularly high risk concerns patients with: complete, partial and mixed gonadal dysgenesis.•Patients with CAIS and Klinefelter syndrome have higher risk of somatic cell neoplasia in gonads.•Adult patient...

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Veröffentlicht in:Cancer epidemiology 2020-12, Vol.69, p.101800-101800, Article 101800
Hauptverfasser: Slowikowska-Hilczer, Jolanta, Szarras-Czapnik, Maria, Duranteau, Lise, Rapp, Marion, Walczak-Jedrzejowska, Renata, Marchlewska, Katarzyna, Oszukowska, Elzbieta, Nordenstrom, Anna
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Sprache:eng
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Zusammenfassung:•Patients with DSD and the Y chromosome have the highest risk of gonadal germ cell neoplasia.•Particularly high risk concerns patients with: complete, partial and mixed gonadal dysgenesis.•Patients with CAIS and Klinefelter syndrome have higher risk of somatic cell neoplasia in gonads.•Adult patients with gonadal dysgenesis and the Y chromosome should be under thorough medical control. Patients with disorders/differences of sex development (DSD), especially those possessing the Y chromosome, have a higher risk of gonadal germ-cell tumours (GCTs). We aimed to examine the incidence of different types of gonadal neoplasia and associated risk factors. A total of 1040 DSD patients aged ≥16 years participated in a cross-sectional multicentre European study (dsd-LIFE). Data on medical history were gathered from the patients’ archival medical documents. A web-based questionnaire was filled out individually by the participants. A physical examination was performed in all, while ultrasonography of gonads was carried out in 214 and semen analysis was performed for 53 patients. Germ-cell neoplasia was present in 12 % of patients with DSD and in 14 % of those with XY DSD. The highest risk (36 %) was observed in 46,XY patients with gonadal dysgenesis (GD): complete GD (33 %) and partial GD (23 %), but also in mixed GD (8 %) and complete androgen insensitivity syndrome (AIS) (6%). It was not reported in partial AIS, XX male, 46,XX DSD and congenital adrenal hyperplasia, Turner and Klinefelter syndromes, or in androgen biosynthesis defects. Benign sex cord-stromal tumours (Sertoli- and Leydig-cell tumours) were noted only in patients with complete AIS (3.1 %) and Klinefelter syndrome (14.3 %). A relationship between risk factors for GCT and gonadal neoplasia appearance, other than the Y chromosome, was not found. Adult patients with GD and the Y chromosome have the highest risk of GCT and should be kept under thorough medical control and receive special medical follow-up to prevent the development of gonadal tumours.
ISSN:1877-7821
1877-783X
1877-783X
DOI:10.1016/j.canep.2020.101800