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Author Notes:

David C. Adamson, cory.adamson@emory.edu

Conceptualization, S.B. and D.C.A.; writing—original draft preparation, S.B.; writing—review and editing, D.C.A. All authors have read and agreed to the published version of the manuscript.

The authors declare no conflict of interest.

Subject:

Research Funding:

This research received no external funding.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Biochemistry & Molecular Biology
  • Medicine, Research & Experimental
  • Pharmacology & Pharmacy
  • Research & Experimental Medicine
  • pituitary adenoma
  • prolactinoma
  • acromegaly
  • Cushing's
  • transsphenoidal
  • CNS tumor
  • DOPAMINE AGONIST THERAPY
  • BILATERAL LAPAROSCOPIC ADRENALECTOMY
  • REPEAT TRANSSPHENOIDAL SURGERY
  • SECONDARY TRANSNASAL SURGERY
  • RADIATION-THERAPY
  • CUSHINGS-SYNDROME
  • CLINICAL-MANIFESTATIONS
  • SOMATOSTATIN ANALOGS
  • MEDICAL PROGRESS
  • HEART-DISEASE

Pituitary Adenomas: From Diagnosis to Therapeutics

Tools:

Journal Title:

BIOMEDICINES

Volume:

Volume 9, Number 5

Publisher:

Type of Work:

Article | Final Publisher PDF

Abstract:

Pituitary adenomas are tumors that arise in the anterior pituitary gland. They are the third most common cause of central nervous system (CNS) tumors among adults. Most adenomas are benign and exert their effect via excess hormone secretion or mass effect. Clinical presentation of pituitary adenoma varies based on their size and hormone secreted. Here, we review some of the most common types of pituitary adenomas, their clinical presentation, and current diagnostic and therapeutic strategies.

Copyright information:

© 2021 by the authors.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/rdf).
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