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Italian Association of Clinical Endocrinologists (AME) and Italian AACE Chapter Position Statement for Clinical Practice: Acromegaly - Part 1: Diagnostic and Clinical Issues

Acromegaly is a rare disease. Improvements in lifespan in these patients have recently been reported due to transsphenoidal surgery (TSS), advances in medical therapy, and strict criteria for defining disease remission. This document reports the opinions of a group of Italian experts who have gather...

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Detalles Bibliográficos
Autores principales: Cozzi, Renato, Ambrosio, Maria R., Attanasio, Roberto, Bozzao, Alessandro, De Marinis, Laura, De Menis, Ernesto, Guastamacchia, Edoardo, Lania, Andrea, Lasio, Giovanni, Logoluso, Francesco, Maffei, Pietro, Poggi, Maurizio, Toscano, Vincenzo, Zini, Michele, Chanson, Philippe, Katznelson, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579251/
https://www.ncbi.nlm.nih.gov/pubmed/31985386
http://dx.doi.org/10.2174/1871530320666200127103320
Descripción
Sumario:Acromegaly is a rare disease. Improvements in lifespan in these patients have recently been reported due to transsphenoidal surgery (TSS), advances in medical therapy, and strict criteria for defining disease remission. This document reports the opinions of a group of Italian experts who have gathered together their prolonged clinical experience in the diagnostic and therapeutic challenges of acromegaly patients. Both GH and IGF-I (only IGF-I in those treated with Pegvisomant) are needed in the diagnosis and follow-up. Comorbidities (cardio-cerebrovascular disease, sleep apnea, metabolic derangement, neoplasms, and bone/joint disease) should be specifically addressed. Any newly diagnosed patient should be referred to a multidisciplinary team experienced in the treatment of pituitary adenomas.