Leydig Cell Hyperplasia Mimicking a Testicular Tumour in a Patient with Klinefelter Syndrome

BACKGROUND: Klinefelter syndrome (KS) is the most common sex-chromosomal disorder in males. Frequently under-recognized, it occurs in 1 in 500–600 male births. It is caused by the inheritance of at least one additional X chromosome from either parent. Patients often have uncommon or atypical maligna...

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Detalles Bibliográficos
Autores principales: Newman, Christine, Connolly, Stephen, MacEneaney, Owen, O’Keane, Conor, McQuaid, Siobhan E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601694/
https://www.ncbi.nlm.nih.gov/pubmed/31293996
http://dx.doi.org/10.12890/2019_001129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601694/
https://www.ncbi.nlm.nih.gov/pubmed/31293996
http://dx.doi.org/10.12890/2019_001129

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