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NUT midline carcinoma in a young pregnant female: a case report

INTRODUCTION: The NUT midline carcinoma is a rare tumor mostly reported in the midline of upper aerodigestive tract and mediastinum. Children as well as adolescents are affected without a gender distribution. A standard treatment is not established. So far, there exists no reported case of a pregnan...

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Autores principales: Joel, Sebastian, Weschenfelder, Friederike, Schleussner, Ekkehard, Hofmann, Gunther O., Weschenfelder, Wolfram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648955/
https://www.ncbi.nlm.nih.gov/pubmed/33160369
http://dx.doi.org/10.1186/s12957-020-02065-6
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author Joel, Sebastian
Weschenfelder, Friederike
Schleussner, Ekkehard
Hofmann, Gunther O.
Weschenfelder, Wolfram
author_facet Joel, Sebastian
Weschenfelder, Friederike
Schleussner, Ekkehard
Hofmann, Gunther O.
Weschenfelder, Wolfram
author_sort Joel, Sebastian
collection PubMed
description INTRODUCTION: The NUT midline carcinoma is a rare tumor mostly reported in the midline of upper aerodigestive tract and mediastinum. Children as well as adolescents are affected without a gender distribution. A standard treatment is not established. So far, there exists no reported case of a pregnant female suffering from NUT midline carcinoma with musculoskeletal manifestation. CASE PRESENTATION: A 34-year-old woman was referred to our outpatient clinic by the general practitioner during her 31st week of pregnancy suffering from shoulder pain and dyspnea. So far, dyspnea was interpreted as a typical pregnancy-related symptom. However, a chest X-ray showed a tumor mass in the right lung in close relation to the scapula. Further examinations found metastases in different areas of the body. No pregnancy-related complications were detected by obstetric examination. After an interdisciplinary perinatal case discussion, cesarean section was directly followed by an open biopsy of the right side scapula tumor lesion. A NUT midline carcinoma was diagnosed by immunohistochemistry. Due to disseminated tumor disease in multiple non-resectable locations, a palliative systemical chemotherapy was started by the oncological outpatient clinic. CONCLUSION: This report presents the case of the very rare NUT midline carcinoma under pregnancy which made interdisciplinary case discussions indispensable for therapy planning.
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spelling pubmed-76489552020-11-09 NUT midline carcinoma in a young pregnant female: a case report Joel, Sebastian Weschenfelder, Friederike Schleussner, Ekkehard Hofmann, Gunther O. Weschenfelder, Wolfram World J Surg Oncol Case Report INTRODUCTION: The NUT midline carcinoma is a rare tumor mostly reported in the midline of upper aerodigestive tract and mediastinum. Children as well as adolescents are affected without a gender distribution. A standard treatment is not established. So far, there exists no reported case of a pregnant female suffering from NUT midline carcinoma with musculoskeletal manifestation. CASE PRESENTATION: A 34-year-old woman was referred to our outpatient clinic by the general practitioner during her 31st week of pregnancy suffering from shoulder pain and dyspnea. So far, dyspnea was interpreted as a typical pregnancy-related symptom. However, a chest X-ray showed a tumor mass in the right lung in close relation to the scapula. Further examinations found metastases in different areas of the body. No pregnancy-related complications were detected by obstetric examination. After an interdisciplinary perinatal case discussion, cesarean section was directly followed by an open biopsy of the right side scapula tumor lesion. A NUT midline carcinoma was diagnosed by immunohistochemistry. Due to disseminated tumor disease in multiple non-resectable locations, a palliative systemical chemotherapy was started by the oncological outpatient clinic. CONCLUSION: This report presents the case of the very rare NUT midline carcinoma under pregnancy which made interdisciplinary case discussions indispensable for therapy planning. BioMed Central 2020-11-07 /pmc/articles/PMC7648955/ /pubmed/33160369 http://dx.doi.org/10.1186/s12957-020-02065-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Case Report
Joel, Sebastian
Weschenfelder, Friederike
Schleussner, Ekkehard
Hofmann, Gunther O.
Weschenfelder, Wolfram
NUT midline carcinoma in a young pregnant female: a case report
title NUT midline carcinoma in a young pregnant female: a case report
title_full NUT midline carcinoma in a young pregnant female: a case report
title_fullStr NUT midline carcinoma in a young pregnant female: a case report
title_full_unstemmed NUT midline carcinoma in a young pregnant female: a case report
title_short NUT midline carcinoma in a young pregnant female: a case report
title_sort nut midline carcinoma in a young pregnant female: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648955/
https://www.ncbi.nlm.nih.gov/pubmed/33160369
http://dx.doi.org/10.1186/s12957-020-02065-6
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