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First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications
BACKGROUND: The PTEN-hamartoma-tumor-syndrome (PHTS) is caused by germline mutations in Phosphatase and Tensin homolog (PTEN) and predisposes to the development of several typical malignancies. Whereas PTEN mutations have been implicated in the occurrence of malignant mesotheliomas, the genetic land...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094911/ https://www.ncbi.nlm.nih.gov/pubmed/30111295 http://dx.doi.org/10.1186/s12881-018-0651-4 |
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author | Löffler, Markus W. Steinhilber, Julia Hilke, Franz J. Haen, Sebastian P. Bösmüller, Hans Montes-Mojarro, Ivonne-Aidee Bonzheim, Irina Stäbler, Antje Faust, Ulrike Grasshoff, Ute Königsrainer, Ingmar Rammensee, Hans-Georg Kanz, Lothar Königsrainer, Alfred Beckert, Stefan Riess, Olaf Schroeder, Christopher |
author_facet | Löffler, Markus W. Steinhilber, Julia Hilke, Franz J. Haen, Sebastian P. Bösmüller, Hans Montes-Mojarro, Ivonne-Aidee Bonzheim, Irina Stäbler, Antje Faust, Ulrike Grasshoff, Ute Königsrainer, Ingmar Rammensee, Hans-Georg Kanz, Lothar Königsrainer, Alfred Beckert, Stefan Riess, Olaf Schroeder, Christopher |
author_sort | Löffler, Markus W. |
collection | PubMed |
description | BACKGROUND: The PTEN-hamartoma-tumor-syndrome (PHTS) is caused by germline mutations in Phosphatase and Tensin homolog (PTEN) and predisposes to the development of several typical malignancies. Whereas PTEN mutations have been implicated in the occurrence of malignant mesotheliomas, the genetic landscape of verrucous carcinomas (VC) is largely uncharted. Both VC and malignant peritoneal mesotheliomas (MPM) are exceedingly rare and a potential link between these malignancies and PHTS has never been reported. CASE PRESENTATION: We here describe the clinical course of a PHTS patient who, in addition to a typical thyroid carcinoma at the age of 36 years, developed a highly-differentiated oral VC and an epithelioid MPM six years later. The patient with a history of occupational asbestos exposure underwent cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for MPM. The clinical diagnosis of PHTS was consequently corroborated by a germline PTEN deletion. Sequencing of tumor tissue revealed a second hit in PTEN in the thyroid carcinoma and VC, confirmed by a PTEN loss and activation of the PI3K/AKT pathway in immunohistochemistry. Furthermore, additional somatic mutations in the thyroid carcinoma as well as in the VC were detected, whereas the genetics of MPM remained unrevealing. DISCUSSION AND CONCLUSIONS: We here report the very unusual clinical course of a patient with rare tumors that have a germline mutation first hit in PTEN in common. Since this patient was exposed to asbestos and current evidence suggests molecular mechanisms that might render PHTS patients particularly susceptible to mesothelioma, we strongly recommend PHTS patients to avoid even minimal exposure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0651-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6094911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60949112018-08-24 First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications Löffler, Markus W. Steinhilber, Julia Hilke, Franz J. Haen, Sebastian P. Bösmüller, Hans Montes-Mojarro, Ivonne-Aidee Bonzheim, Irina Stäbler, Antje Faust, Ulrike Grasshoff, Ute Königsrainer, Ingmar Rammensee, Hans-Georg Kanz, Lothar Königsrainer, Alfred Beckert, Stefan Riess, Olaf Schroeder, Christopher BMC Med Genet Case Report BACKGROUND: The PTEN-hamartoma-tumor-syndrome (PHTS) is caused by germline mutations in Phosphatase and Tensin homolog (PTEN) and predisposes to the development of several typical malignancies. Whereas PTEN mutations have been implicated in the occurrence of malignant mesotheliomas, the genetic landscape of verrucous carcinomas (VC) is largely uncharted. Both VC and malignant peritoneal mesotheliomas (MPM) are exceedingly rare and a potential link between these malignancies and PHTS has never been reported. CASE PRESENTATION: We here describe the clinical course of a PHTS patient who, in addition to a typical thyroid carcinoma at the age of 36 years, developed a highly-differentiated oral VC and an epithelioid MPM six years later. The patient with a history of occupational asbestos exposure underwent cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for MPM. The clinical diagnosis of PHTS was consequently corroborated by a germline PTEN deletion. Sequencing of tumor tissue revealed a second hit in PTEN in the thyroid carcinoma and VC, confirmed by a PTEN loss and activation of the PI3K/AKT pathway in immunohistochemistry. Furthermore, additional somatic mutations in the thyroid carcinoma as well as in the VC were detected, whereas the genetics of MPM remained unrevealing. DISCUSSION AND CONCLUSIONS: We here report the very unusual clinical course of a patient with rare tumors that have a germline mutation first hit in PTEN in common. Since this patient was exposed to asbestos and current evidence suggests molecular mechanisms that might render PHTS patients particularly susceptible to mesothelioma, we strongly recommend PHTS patients to avoid even minimal exposure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0651-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-15 /pmc/articles/PMC6094911/ /pubmed/30111295 http://dx.doi.org/10.1186/s12881-018-0651-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Case Report Löffler, Markus W. Steinhilber, Julia Hilke, Franz J. Haen, Sebastian P. Bösmüller, Hans Montes-Mojarro, Ivonne-Aidee Bonzheim, Irina Stäbler, Antje Faust, Ulrike Grasshoff, Ute Königsrainer, Ingmar Rammensee, Hans-Georg Kanz, Lothar Königsrainer, Alfred Beckert, Stefan Riess, Olaf Schroeder, Christopher First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications |
title | First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications |
title_full | First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications |
title_fullStr | First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications |
title_full_unstemmed | First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications |
title_short | First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implications |
title_sort | first case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline pten mutation: a combination of extremely rare diseases with probable further implications |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094911/ https://www.ncbi.nlm.nih.gov/pubmed/30111295 http://dx.doi.org/10.1186/s12881-018-0651-4 |
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