Rare association: Mazabraud syndrome and McCune-Albright syndrome

 

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون: López Sáenz, José Gerardo, Leandro Sandí, Verónica
التنسيق: artículo original
الحالة:Versión publicada
تاريخ النشر:2025
الوصف:A 59-year-old female patient with type 2 diabetes mellitus, chronic bone pain and hyperthyroidism without treatment, as well as multiple fractures since childhood, early puberty and recently diagnosed intramuscular myxoma, was admitted to internal medicine unit to establish a clinical syndrome. Imaging and nuclear medicine studies were carried out and polyostotic fibrous dysplasia was documented, which in association with intramuscular myxoma are characteristic of Mazabraud's syndrome. In addition, the correlation between precocious puberty, endocrine dysfunction and a single café-au-lait spot on the back was made, which allowed establishing the clinical diagnosis of McCune-Albright syndrome. The case of the association of these two rare syndromes is presented.
البلد:Portal de Revistas UCR
المؤسسة:Universidad de Costa Rica
Repositorio:Portal de Revistas UCR
اللغة:Español
OAI Identifier:oai:archivo.portal.ucr.ac.cr:article/62239
الوصول للمادة أونلاين:https://archivo.revistas.ucr.ac.cr/index.php/medica/article/view/62239
كلمة مفتاحية:Fibrous dysplasia, polyostotic; mixoma; hyperpigmentation
Displasia fibrosa poliostótica; mixoma; manchas café con leche