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CK19 is a sensitive marker for yolk sac tumours of the testis
BACKGROUND: Malignant germ cell tumours are the most common malignant tumours in young men. They are histologically divided into seminomas and non-seminomas. Non-seminomas are further subdivided into embryonic carcinomas, yolk sac tumours, chorionic carcinomas, and teratomas. For the therapeutic man...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384355/ https://www.ncbi.nlm.nih.gov/pubmed/25889715 http://dx.doi.org/10.1186/s13000-015-0243-y |
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author | Bremmer, Felix Ströbel, Philipp Jarry, Hubertus Strecker, Jasmin Gaisa, Nadine Strauß, Arne Schweyer, Stefan Radzun, Heinz-Joachim Behnes, Carl-Ludwig |
author_facet | Bremmer, Felix Ströbel, Philipp Jarry, Hubertus Strecker, Jasmin Gaisa, Nadine Strauß, Arne Schweyer, Stefan Radzun, Heinz-Joachim Behnes, Carl-Ludwig |
author_sort | Bremmer, Felix |
collection | PubMed |
description | BACKGROUND: Malignant germ cell tumours are the most common malignant tumours in young men. They are histologically divided into seminomas and non-seminomas. Non-seminomas are further subdivided into embryonic carcinomas, yolk sac tumours, chorionic carcinomas, and teratomas. For the therapeutic management it is essential to differentiate between these histological subtypes. METHODS: Investigated cases included normal testis (n = 50), intratubular germ cell neoplasia (n = 25), seminomas (n = 67), embryonic carcinomas (n = 56), yolk sac tumours (n = 29), chorionic carcinomas (n = 2), teratomas (n = 7) and four metastases of YST’s for their CK19 expression. In addition Leydig cell- (n = 10) and Sertoli cell- tumours (n = 4) were included in this study. RESULTS: All investigated seminomas, embryonic carcinomas as well as normal testis and intratubular germ cell neoplasias did not express CK19. In contrast, all investigated yolk sac tumours strongly expressed CK19 protein. These findings became also evident in mixed germ cell tumours consisting of embryonic carcinomas and yolk sac tumours, although CK19-expression could also be observed in analysed chorionic carcinomas and epithelial components of teratomas. CONCLUSION: CK19 proved to be a sensitive marker to identify yolk sac tumours of the testis and to distinguish them from other germ cell tumours, especially seminomas and embryonic carcinomas. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/4075546891400979. |
format | Online Article Text |
id | pubmed-4384355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43843552015-04-04 CK19 is a sensitive marker for yolk sac tumours of the testis Bremmer, Felix Ströbel, Philipp Jarry, Hubertus Strecker, Jasmin Gaisa, Nadine Strauß, Arne Schweyer, Stefan Radzun, Heinz-Joachim Behnes, Carl-Ludwig Diagn Pathol Research BACKGROUND: Malignant germ cell tumours are the most common malignant tumours in young men. They are histologically divided into seminomas and non-seminomas. Non-seminomas are further subdivided into embryonic carcinomas, yolk sac tumours, chorionic carcinomas, and teratomas. For the therapeutic management it is essential to differentiate between these histological subtypes. METHODS: Investigated cases included normal testis (n = 50), intratubular germ cell neoplasia (n = 25), seminomas (n = 67), embryonic carcinomas (n = 56), yolk sac tumours (n = 29), chorionic carcinomas (n = 2), teratomas (n = 7) and four metastases of YST’s for their CK19 expression. In addition Leydig cell- (n = 10) and Sertoli cell- tumours (n = 4) were included in this study. RESULTS: All investigated seminomas, embryonic carcinomas as well as normal testis and intratubular germ cell neoplasias did not express CK19. In contrast, all investigated yolk sac tumours strongly expressed CK19 protein. These findings became also evident in mixed germ cell tumours consisting of embryonic carcinomas and yolk sac tumours, although CK19-expression could also be observed in analysed chorionic carcinomas and epithelial components of teratomas. CONCLUSION: CK19 proved to be a sensitive marker to identify yolk sac tumours of the testis and to distinguish them from other germ cell tumours, especially seminomas and embryonic carcinomas. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/4075546891400979. BioMed Central 2015-03-24 /pmc/articles/PMC4384355/ /pubmed/25889715 http://dx.doi.org/10.1186/s13000-015-0243-y Text en © Bremmer et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Bremmer, Felix Ströbel, Philipp Jarry, Hubertus Strecker, Jasmin Gaisa, Nadine Strauß, Arne Schweyer, Stefan Radzun, Heinz-Joachim Behnes, Carl-Ludwig CK19 is a sensitive marker for yolk sac tumours of the testis |
title | CK19 is a sensitive marker for yolk sac tumours of the testis |
title_full | CK19 is a sensitive marker for yolk sac tumours of the testis |
title_fullStr | CK19 is a sensitive marker for yolk sac tumours of the testis |
title_full_unstemmed | CK19 is a sensitive marker for yolk sac tumours of the testis |
title_short | CK19 is a sensitive marker for yolk sac tumours of the testis |
title_sort | ck19 is a sensitive marker for yolk sac tumours of the testis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384355/ https://www.ncbi.nlm.nih.gov/pubmed/25889715 http://dx.doi.org/10.1186/s13000-015-0243-y |
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