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Phaeochromocytoma in a patient with a Birt-Hogg-Dubé syndrome phenotype
A case of phaeochromocytoma in a female patient in her 50s with phenotypical expressions for the rare Birt-Hogg-Dubé (BHD) syndrome is presented. Whether this is an incidental finding or that there is a composite relationship between these two entities remains to be fully described. Less than 10 cas...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BMJ Publishing Group
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069485/ https://www.ncbi.nlm.nih.gov/pubmed/36997239 http://dx.doi.org/10.1136/bcr-2022-252362 |