Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis

SUMMARY A gonadal tumor was diagnosed in the first months of life in a patient with genital ambiguity, a 45,X/46,XY karyotype, and mixed gonadal dysgenesis. Gonadal biopsies at the age of 3 months revealed dysgenetic testes and a gonadoblastoma on the right testis. Even though gonadal tumors are rar...

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Main Authors: Sarah Crestian Cunha, Juliana Gabriel Ribeiro de Andrade, Camila Matsunaga de Angelis, Athanase Billis, Joaquim Murray Bustorff-Silva, Andréa Trevas Maciel-Guerra, Márcio Lopes Miranda, Gil Guerra-Júnior
Format: Article
Language:English
Published: Brazilian Society of Endocrinology and Metabolism
Series:Archives of Endocrinology and Metabolism
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972018000600644&lng=en&tlng=en
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spelling doaj-5242e789cad94969a7a5b41a7cac854a2020-11-25T01:06:31ZengBrazilian Society of Endocrinology and MetabolismArchives of Endocrinology and Metabolism2359-429262664464710.20945/2359-3997000000091S2359-39972018000600644Early development of a gonadal tumor in a patient with mixed gonadal dysgenesisSarah Crestian CunhaJuliana Gabriel Ribeiro de AndradeCamila Matsunaga de AngelisAthanase BillisJoaquim Murray Bustorff-SilvaAndréa Trevas Maciel-GuerraMárcio Lopes MirandaGil Guerra-JúniorSUMMARY A gonadal tumor was diagnosed in the first months of life in a patient with genital ambiguity, a 45,X/46,XY karyotype, and mixed gonadal dysgenesis. Gonadal biopsies at the age of 3 months revealed dysgenetic testes and a gonadoblastoma on the right testis. Even though gonadal tumors are rare in childhood, this case indicates that prophylactic removal of dysgenetic gonads should be performed as early as possible, especially when the female sex is assigned to a patient with a Y-chromosome sequence.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972018000600644&lng=en&tlng=en
collection DOAJ
language English
format Article
sources DOAJ
author Sarah Crestian Cunha
Juliana Gabriel Ribeiro de Andrade
Camila Matsunaga de Angelis
Athanase Billis
Joaquim Murray Bustorff-Silva
Andréa Trevas Maciel-Guerra
Márcio Lopes Miranda
Gil Guerra-Júnior
spellingShingle Sarah Crestian Cunha
Juliana Gabriel Ribeiro de Andrade
Camila Matsunaga de Angelis
Athanase Billis
Joaquim Murray Bustorff-Silva
Andréa Trevas Maciel-Guerra
Márcio Lopes Miranda
Gil Guerra-Júnior
Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
Archives of Endocrinology and Metabolism
author_facet Sarah Crestian Cunha
Juliana Gabriel Ribeiro de Andrade
Camila Matsunaga de Angelis
Athanase Billis
Joaquim Murray Bustorff-Silva
Andréa Trevas Maciel-Guerra
Márcio Lopes Miranda
Gil Guerra-Júnior
author_sort Sarah Crestian Cunha
title Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
title_short Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
title_full Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
title_fullStr Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
title_full_unstemmed Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
title_sort early development of a gonadal tumor in a patient with mixed gonadal dysgenesis
publisher Brazilian Society of Endocrinology and Metabolism
series Archives of Endocrinology and Metabolism
issn 2359-4292
description SUMMARY A gonadal tumor was diagnosed in the first months of life in a patient with genital ambiguity, a 45,X/46,XY karyotype, and mixed gonadal dysgenesis. Gonadal biopsies at the age of 3 months revealed dysgenetic testes and a gonadoblastoma on the right testis. Even though gonadal tumors are rare in childhood, this case indicates that prophylactic removal of dysgenetic gonads should be performed as early as possible, especially when the female sex is assigned to a patient with a Y-chromosome sequence.
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972018000600644&lng=en&tlng=en
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