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Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female
Solitary fibrous tumors are rare mesenchymal tumors most commonly arising from the pleura. When associated with paraneoplastic syndrome of hypoglycemia caused by the secretion of a high-molecular-weight form of insulin-like growth factor II, it is referred to as the Doege–Potter syndrome. Surgery wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349974/ https://www.ncbi.nlm.nih.gov/pubmed/30719313 http://dx.doi.org/10.1177/2050313X18823468 |
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author | Forster, Céline Roumy, Aurélien Gonzalez, Michel |
author_facet | Forster, Céline Roumy, Aurélien Gonzalez, Michel |
author_sort | Forster, Céline |
collection | PubMed |
description | Solitary fibrous tumors are rare mesenchymal tumors most commonly arising from the pleura. When associated with paraneoplastic syndrome of hypoglycemia caused by the secretion of a high-molecular-weight form of insulin-like growth factor II, it is referred to as the Doege–Potter syndrome. Surgery with complete tumor resection is the only curative treatment. We present here the case of a 93-year-old female diagnosed with a Doege–Potter syndrome who underwent three repetitive surgical resections of recurrent solitary fibrous tumor. |
format | Online Article Text |
id | pubmed-6349974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-63499742019-02-04 Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female Forster, Céline Roumy, Aurélien Gonzalez, Michel SAGE Open Med Case Rep Case Report Solitary fibrous tumors are rare mesenchymal tumors most commonly arising from the pleura. When associated with paraneoplastic syndrome of hypoglycemia caused by the secretion of a high-molecular-weight form of insulin-like growth factor II, it is referred to as the Doege–Potter syndrome. Surgery with complete tumor resection is the only curative treatment. We present here the case of a 93-year-old female diagnosed with a Doege–Potter syndrome who underwent three repetitive surgical resections of recurrent solitary fibrous tumor. SAGE Publications 2019-01-12 /pmc/articles/PMC6349974/ /pubmed/30719313 http://dx.doi.org/10.1177/2050313X18823468 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Forster, Céline Roumy, Aurélien Gonzalez, Michel Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female |
title | Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female |
title_full | Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female |
title_fullStr | Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female |
title_full_unstemmed | Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female |
title_short | Solitary fibrous tumor of the pleura with Doege–Potter syndrome: Second recurrence in a 93-year-old female |
title_sort | solitary fibrous tumor of the pleura with doege–potter syndrome: second recurrence in a 93-year-old female |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349974/ https://www.ncbi.nlm.nih.gov/pubmed/30719313 http://dx.doi.org/10.1177/2050313X18823468 |
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