Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation
Glucagonoma is a neuroendocrine tumour of very low incidence, estimated at 1 case per 20 million people per year. It typically manifests with a clinical syndrome that includes a characteristic dermatosis called necrolytic migratory erythema (NME). We present the case of a 60-year-old male with NME a...
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| Formato: | Artículo revista |
| Lenguaje: | Español |
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Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología
2022
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| Acceso en línea: | https://revistas.unc.edu.ar/index.php/med/article/view/32543 |
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I10-R327-article-325432022-08-19T21:47:05Z Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation Eritema necrolítico migratorio como manifestación de tumor neuroendocrino de páncreas. Valoración clínico-radiológica Eritema necrólito migratório como manifestação de tumor neuroendócrino pancreático. Avaliação clínico-radiológica Dulcich, Gonzalo Mestas Nuñez, Marcos Alejandro Gentile, Ernestina Maria Jose glucagonoma necrolytic migratory erythema neuroendocrine tumors glucagonoma eritema necrolítico migratorio tumores neuroendocrinos glucagonoma eritema migratório necrolítico tumores neuroendócrinos Glucagonoma is a neuroendocrine tumour of very low incidence, estimated at 1 case per 20 million people per year. It typically manifests with a clinical syndrome that includes a characteristic dermatosis called necrolytic migratory erythema (NME). We present the case of a 60-year-old male with NME as the initial presentation of a pancreatic tumour and its imaging findings. We emphasize the importance of recognizing the clinical features of NME and the role of different imaging methods for early diagnosis and correct management of these pancreatic tumours. El glucagonoma es un tumor neuroendocrino de muy baja incidencia, se estima 1 caso cada 20 millones de personas por año. Típicamente, se manifiesta con un síndrome clínico que incluye una dermatosis característica denominada eritema necrolítico migratorio (ENM). Presentamos el caso de un varón de 60 años con ENM como presentación inicial de un tumor pancreático y los hallazgos por imágenes del mismo. Resaltamos la importancia de reconocer las características clínicas del ENM y el rol de los diferentes métodos por imágenes para un diagnóstico precoz y correcto manejo de estos tumores pancreáticos. O glucagonoma é um tumor neuroendócrino de incidência muito baixa, estimado em 1 caso por 20 milhões de pessoas por ano. Tipicamente, manifesta-se com uma síndrome clínica que inclui uma dermatose característica chamada eritema necróltico migrans (ENM). Apresentamos o caso de um homem de 60 anos de idade com ENM como a apresentação inicial de um tumor pancreático e seus achados de imagem. Destacamos a importância de reconhecer as características clínicas do ENM e o papel dos diferentes métodos de imagem para o diagnóstico precoce e o manejo correto desses tumores pancreáticos. Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología 2022-06-06 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion application/pdf text/html https://revistas.unc.edu.ar/index.php/med/article/view/32543 10.31053/1853.0605.v79.n2.32543 Revista de la Facultad de Ciencias Médicas de Córdoba.; Vol. 79 No. 2 (2022); 188-192 Revista de la Facultad de Ciencias Médicas de Córdoba; Vol. 79 Núm. 2 (2022); 188-192 Revista da Faculdade de Ciências Médicas de Córdoba; v. 79 n. 2 (2022); 188-192 1853-0605 0014-6722 10.31053/1853.0605.v79.n2 spa https://revistas.unc.edu.ar/index.php/med/article/view/32543/37943 https://revistas.unc.edu.ar/index.php/med/article/view/32543/37518 Derechos de autor 2022 Universidad Nacional de Córdoba http://creativecommons.org/licenses/by-nc/4.0 |
| institution |
Universidad Nacional de Córdoba |
| institution_str |
I-10 |
| repository_str |
R-327 |
| container_title_str |
Revista de la Facultad de Ciencias Médicas de Córdoba |
| language |
Español |
| format |
Artículo revista |
| topic |
glucagonoma necrolytic migratory erythema neuroendocrine tumors glucagonoma eritema necrolítico migratorio tumores neuroendocrinos glucagonoma eritema migratório necrolítico tumores neuroendócrinos |
| spellingShingle |
glucagonoma necrolytic migratory erythema neuroendocrine tumors glucagonoma eritema necrolítico migratorio tumores neuroendocrinos glucagonoma eritema migratório necrolítico tumores neuroendócrinos Dulcich, Gonzalo Mestas Nuñez, Marcos Alejandro Gentile, Ernestina Maria Jose Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation |
| topic_facet |
glucagonoma necrolytic migratory erythema neuroendocrine tumors glucagonoma eritema necrolítico migratorio tumores neuroendocrinos glucagonoma eritema migratório necrolítico tumores neuroendócrinos |
| author |
Dulcich, Gonzalo Mestas Nuñez, Marcos Alejandro Gentile, Ernestina Maria Jose |
| author_facet |
Dulcich, Gonzalo Mestas Nuñez, Marcos Alejandro Gentile, Ernestina Maria Jose |
| author_sort |
Dulcich, Gonzalo |
| title |
Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation |
| title_short |
Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation |
| title_full |
Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation |
| title_fullStr |
Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation |
| title_full_unstemmed |
Migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. Clinical-radiological evaluation |
| title_sort |
migratory necrolytic erythema as a manifestation of pancreatic neuroendocrine tumor. clinical-radiological evaluation |
| description |
Glucagonoma is a neuroendocrine tumour of very low incidence, estimated at 1 case per 20 million people per year. It typically manifests with a clinical syndrome that includes a characteristic dermatosis called necrolytic migratory erythema (NME). We present the case of a 60-year-old male with NME as the initial presentation of a pancreatic tumour and its imaging findings. We emphasize the importance of recognizing the clinical features of NME and the role of different imaging methods for early diagnosis and correct management of these pancreatic tumours. |
| publisher |
Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología |
| publishDate |
2022 |
| url |
https://revistas.unc.edu.ar/index.php/med/article/view/32543 |
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