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Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?

BACKGROUND: Family history is among the few established risk factors for testicular germ cell tumor (TGCT). Approximately 1.4% of newly diagnosed TGCT patients report a positive family history of TGCT. Sons and siblings of TGCT patients have four- to six fold and eight- to tenfold increase in TGCT r...

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Autores principales: Guindalini, Rodrigo Santa Cruz, de Oliveira, Edite Paulo, Silvino, Marina Cavalcanto Moroja, Hoff, Paulo Marcelo, Garicochea, Bernardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599932/
https://www.ncbi.nlm.nih.gov/pubmed/23510634
http://dx.doi.org/10.1186/1897-4287-11-1
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author Guindalini, Rodrigo Santa Cruz
de Oliveira, Edite Paulo
Silvino, Marina Cavalcanto Moroja
Hoff, Paulo Marcelo
Garicochea, Bernardo
author_facet Guindalini, Rodrigo Santa Cruz
de Oliveira, Edite Paulo
Silvino, Marina Cavalcanto Moroja
Hoff, Paulo Marcelo
Garicochea, Bernardo
author_sort Guindalini, Rodrigo Santa Cruz
collection PubMed
description BACKGROUND: Family history is among the few established risk factors for testicular germ cell tumor (TGCT). Approximately 1.4% of newly diagnosed TGCT patients report a positive family history of TGCT. Sons and siblings of TGCT patients have four- to six fold and eight- to tenfold increase in TGCT risk, respectively. In twins of men with TGCT the relative risk of testicular cancer is 37.5 (12.3-115.6). Nevertheless, information about the occurrence of TGCT in relatives of patients with extragonadal germ cell tumor is limited. CASE REPORT: A 24 year-old male patient was diagnosed with a mediastinum tumor and was submitted to image-guided biopsy, which revealed a seminoma. Two months later, his non-identical asymptomatic twin brother was submitted to an elective ultrasound of the testes, which showed a left testicular mass of 4.2 cm. This patient underwent orchiectomy revealing a seminoma of the left testis. There are no other cases of seminoma or other types of cancers reported in first-degree relatives in this family. CONCLUSIONS: Although familial aggregations of TGCT have been well described, to the best of our knowledge, no data concerning the association of gonadal and extragonadal germ cell tumor in relatives has been previously reported. Further investigation on this association is warranted and may help in improving our knowledge of familial pattern inheritance.
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spelling pubmed-35999322013-03-17 Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors? Guindalini, Rodrigo Santa Cruz de Oliveira, Edite Paulo Silvino, Marina Cavalcanto Moroja Hoff, Paulo Marcelo Garicochea, Bernardo Hered Cancer Clin Pract Case Report BACKGROUND: Family history is among the few established risk factors for testicular germ cell tumor (TGCT). Approximately 1.4% of newly diagnosed TGCT patients report a positive family history of TGCT. Sons and siblings of TGCT patients have four- to six fold and eight- to tenfold increase in TGCT risk, respectively. In twins of men with TGCT the relative risk of testicular cancer is 37.5 (12.3-115.6). Nevertheless, information about the occurrence of TGCT in relatives of patients with extragonadal germ cell tumor is limited. CASE REPORT: A 24 year-old male patient was diagnosed with a mediastinum tumor and was submitted to image-guided biopsy, which revealed a seminoma. Two months later, his non-identical asymptomatic twin brother was submitted to an elective ultrasound of the testes, which showed a left testicular mass of 4.2 cm. This patient underwent orchiectomy revealing a seminoma of the left testis. There are no other cases of seminoma or other types of cancers reported in first-degree relatives in this family. CONCLUSIONS: Although familial aggregations of TGCT have been well described, to the best of our knowledge, no data concerning the association of gonadal and extragonadal germ cell tumor in relatives has been previously reported. Further investigation on this association is warranted and may help in improving our knowledge of familial pattern inheritance. BioMed Central 2013-03-04 /pmc/articles/PMC3599932/ /pubmed/23510634 http://dx.doi.org/10.1186/1897-4287-11-1 Text en Copyright ©2013 Guindalini et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Guindalini, Rodrigo Santa Cruz
de Oliveira, Edite Paulo
Silvino, Marina Cavalcanto Moroja
Hoff, Paulo Marcelo
Garicochea, Bernardo
Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
title Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
title_full Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
title_fullStr Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
title_full_unstemmed Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
title_short Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
title_sort should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599932/
https://www.ncbi.nlm.nih.gov/pubmed/23510634
http://dx.doi.org/10.1186/1897-4287-11-1
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