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Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome

CONTEXT: McCune-Albright syndrome (MAS) is caused by sporadic mutations of the GNAS. Patients exhibit features of acromegaly. In most patients, GH-secreting pituitary adenomas have been held responsible for this presentation. However, surgical adenomectomy rarely eliminates excess GH production. OBJ...

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Autores principales: Vortmeyer, Alexander O., Gläsker, Sven, Mehta, Gautam U., Abu-Asab, Mones S., Smith, Jonathan H., Zhuang, Zhengping, Collins, Michael T., Oldfield, Edward H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791436/
https://www.ncbi.nlm.nih.gov/pubmed/22564667
http://dx.doi.org/10.1210/jc.2012-1274
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author Vortmeyer, Alexander O.
Gläsker, Sven
Mehta, Gautam U.
Abu-Asab, Mones S.
Smith, Jonathan H.
Zhuang, Zhengping
Collins, Michael T.
Oldfield, Edward H.
author_facet Vortmeyer, Alexander O.
Gläsker, Sven
Mehta, Gautam U.
Abu-Asab, Mones S.
Smith, Jonathan H.
Zhuang, Zhengping
Collins, Michael T.
Oldfield, Edward H.
author_sort Vortmeyer, Alexander O.
collection PubMed
description CONTEXT: McCune-Albright syndrome (MAS) is caused by sporadic mutations of the GNAS. Patients exhibit features of acromegaly. In most patients, GH-secreting pituitary adenomas have been held responsible for this presentation. However, surgical adenomectomy rarely eliminates excess GH production. OBJECTIVE: The aim of this study was to elucidate pituitary pathology in patients with MAS and to explain the basis of failure of adenomectomy to eliminate GH hypersecretion. DESIGN AND SETTING: We conducted a case series at the National Institutes of Health. INTERVENTION(S): Interventions included medical therapy and transsphenoidal surgery. PATIENTS AND MAIN OUTCOME MEASURES: We studied clinical and imaging features and the histology and molecular features of the pituitary of four acromegalic MAS patients. RESULTS: We identified widespread and diffuse pituitary gland disease. The primary pathological changes were characterized by hyperplastic and neoplastic change, associated with overrepresentation of somatotroph cells in structurally intact tissue areas. Genetic analysis of multiple microdissected samples of any type of histological area consistently revealed identical GNAS mutations in individual patients. The only patient with remission after surgery received complete hypophysectomy in addition to removal of multiple GH-secreting tumors. CONCLUSIONS: These findings indicate developmental effects of GNAS mutation on the entire anterior pituitary gland. The pituitary of individual cases contains a spectrum of changes with regions of normal appearing gland, hyperplasia, and areas of fully developed adenoma formation, as well as transitional stages between these entities. The primary change underlying acromegaly in MAS patients is somatotroph hyperplasia involving the entire pituitary gland, with or without development of somatotroph adenoma. Thus, successful clinical management, whether it is medical, surgical, or via irradiation, must target the entire pituitary, not just the adenomas evident on imaging.
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spelling pubmed-37914362013-11-01 Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome Vortmeyer, Alexander O. Gläsker, Sven Mehta, Gautam U. Abu-Asab, Mones S. Smith, Jonathan H. Zhuang, Zhengping Collins, Michael T. Oldfield, Edward H. J Clin Endocrinol Metab Endocrine Care CONTEXT: McCune-Albright syndrome (MAS) is caused by sporadic mutations of the GNAS. Patients exhibit features of acromegaly. In most patients, GH-secreting pituitary adenomas have been held responsible for this presentation. However, surgical adenomectomy rarely eliminates excess GH production. OBJECTIVE: The aim of this study was to elucidate pituitary pathology in patients with MAS and to explain the basis of failure of adenomectomy to eliminate GH hypersecretion. DESIGN AND SETTING: We conducted a case series at the National Institutes of Health. INTERVENTION(S): Interventions included medical therapy and transsphenoidal surgery. PATIENTS AND MAIN OUTCOME MEASURES: We studied clinical and imaging features and the histology and molecular features of the pituitary of four acromegalic MAS patients. RESULTS: We identified widespread and diffuse pituitary gland disease. The primary pathological changes were characterized by hyperplastic and neoplastic change, associated with overrepresentation of somatotroph cells in structurally intact tissue areas. Genetic analysis of multiple microdissected samples of any type of histological area consistently revealed identical GNAS mutations in individual patients. The only patient with remission after surgery received complete hypophysectomy in addition to removal of multiple GH-secreting tumors. CONCLUSIONS: These findings indicate developmental effects of GNAS mutation on the entire anterior pituitary gland. The pituitary of individual cases contains a spectrum of changes with regions of normal appearing gland, hyperplasia, and areas of fully developed adenoma formation, as well as transitional stages between these entities. The primary change underlying acromegaly in MAS patients is somatotroph hyperplasia involving the entire pituitary gland, with or without development of somatotroph adenoma. Thus, successful clinical management, whether it is medical, surgical, or via irradiation, must target the entire pituitary, not just the adenomas evident on imaging. Endocrine Society 2012-07 2012-05-07 /pmc/articles/PMC3791436/ /pubmed/22564667 http://dx.doi.org/10.1210/jc.2012-1274 Text en Copyright © 2012 by The Endocrine Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/us/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Endocrine Care
Vortmeyer, Alexander O.
Gläsker, Sven
Mehta, Gautam U.
Abu-Asab, Mones S.
Smith, Jonathan H.
Zhuang, Zhengping
Collins, Michael T.
Oldfield, Edward H.
Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome
title Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome
title_full Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome
title_fullStr Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome
title_full_unstemmed Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome
title_short Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome
title_sort somatic gnas mutation causes widespread and diffuse pituitary disease in acromegalic patients with mccune-albright syndrome
topic Endocrine Care
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791436/
https://www.ncbi.nlm.nih.gov/pubmed/22564667
http://dx.doi.org/10.1210/jc.2012-1274
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