Surgical treatment and follow-up results of pituitary ACTH microadenoma: 18 years' experience

Weiguo Zhao1, Shikuen Zhan, Yu Cai

  • 1Department of Neurosurgery, Rui Jin Hospital of Shanghai Second Medical University, Shanghai, People's Republic of China. rjneurosurgery@yahoo.com.cn

Asian Journal of Surgery
|January 16, 2003
PubMed
Abstract

Insights

Surgical treatment of pituitary adrenocorticotropic hormone (ACTH) microadenomas shows high remission rates, particularly for grade 0 tumors. Clinical findings and dexamethasone testing are crucial for diagnosing ACTH grade 0 microadenomas.

Area of Science:

  • Endocrinology
  • Neurosurgery
  • Oncology

Background:

  • Pituitary adrenocorticotropic hormone (ACTH) microadenomas are small tumors.
  • Accurate diagnosis and effective treatment are essential for patient outcomes.

Purpose of the Study:

  • To review clinical experience with surgical treatment and follow-up of pituitary ACTH microadenomas.
  • To evaluate the effectiveness of the transsphenoidal approach for these tumors.

Main Methods:

  • Retrospective review of 87 patients with ACTH microadenomas treated surgically.
  • Transsphenoidal surgery was performed.
  • Preoperative imaging and dexamethasone suppression testing were utilized.

Main Results:

  • Histological confirmation of ACTH microadenoma in all 87 cases.
  • Remission rates were 82% for grade I and 92% for grade 0 microadenomas.
  • High-dose dexamethasone suppression testing was positive in 86% of patients.

Conclusions:

  • Neuroimaging has limited value for diagnosing ACTH grade 0 microadenoma.
  • Clinical manifestation and positive dexamethasone suppression testing are decisive for diagnosis.
  • Surgical intervention achieves high remission rates, especially for grade 0 ACTH microadenomas.

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