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Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion
Doege‐Potter syndrome is a rare hypoglycemic paraneoplastic disorder. This case describes that severe and symptomatic hypoglycemia can occasionally be due to a rare malignant neoplasm, and the differential diagnosis of malignancy should not be overlooked in this setting.
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222743/ https://www.ncbi.nlm.nih.gov/pubmed/34194795 http://dx.doi.org/10.1002/ccr3.4291 |
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author | Fort‐Culillas, Roser Barahona San Millán, Rebeca Garcia‐Fructuoso, Isabel Quera González, Angels Grau Martín, Armand Puigdemont Guinart, Montserrat Rubió‐Casadevall, Jordi Recasens Sala, Mònica Porta Balanyà, Rut |
author_facet | Fort‐Culillas, Roser Barahona San Millán, Rebeca Garcia‐Fructuoso, Isabel Quera González, Angels Grau Martín, Armand Puigdemont Guinart, Montserrat Rubió‐Casadevall, Jordi Recasens Sala, Mònica Porta Balanyà, Rut |
author_sort | Fort‐Culillas, Roser |
collection | PubMed |
description | Doege‐Potter syndrome is a rare hypoglycemic paraneoplastic disorder. This case describes that severe and symptomatic hypoglycemia can occasionally be due to a rare malignant neoplasm, and the differential diagnosis of malignancy should not be overlooked in this setting. |
format | Online Article Text |
id | pubmed-8222743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82227432021-06-29 Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion Fort‐Culillas, Roser Barahona San Millán, Rebeca Garcia‐Fructuoso, Isabel Quera González, Angels Grau Martín, Armand Puigdemont Guinart, Montserrat Rubió‐Casadevall, Jordi Recasens Sala, Mònica Porta Balanyà, Rut Clin Case Rep Case Reports Doege‐Potter syndrome is a rare hypoglycemic paraneoplastic disorder. This case describes that severe and symptomatic hypoglycemia can occasionally be due to a rare malignant neoplasm, and the differential diagnosis of malignancy should not be overlooked in this setting. John Wiley and Sons Inc. 2021-06-23 /pmc/articles/PMC8222743/ /pubmed/34194795 http://dx.doi.org/10.1002/ccr3.4291 Text en © 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Fort‐Culillas, Roser Barahona San Millán, Rebeca Garcia‐Fructuoso, Isabel Quera González, Angels Grau Martín, Armand Puigdemont Guinart, Montserrat Rubió‐Casadevall, Jordi Recasens Sala, Mònica Porta Balanyà, Rut Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion |
title | Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion |
title_full | Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion |
title_fullStr | Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion |
title_full_unstemmed | Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion |
title_short | Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion |
title_sort | doege‐potter syndrome in a facial solitary fibrous tumor: diagnose and clinical management discussion |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222743/ https://www.ncbi.nlm.nih.gov/pubmed/34194795 http://dx.doi.org/10.1002/ccr3.4291 |
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