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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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.
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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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