Surgical Outcomes of Silent ACTH+ Corticotroph Pituitary Neuroendocrine Tumors: A Multi-Institutional Experience and Review of the Literature

Silent corticotroph PitNETs have high rates of extrasellar growth, often limiting the ability to achieve gross total resection. Recurrence/progression is common, occurring in 13% to 17% of cases within two years, necessitating the need for close postoperative follow-up.

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Publication Details

Journal
Neurosurgery
Published
2025-05-15
DOI
https://doi.org/10.1227/neu.0000000000003512
Citations
1
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
Field-Weighted Citation Impact
1.29
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article

Surgical Outcomes of Silent ACTH+ Corticotroph Pituitary Neuroendocrine Tumors: A Multi-Institutional Experience and Review of the Literature

Jacob Ruzevick, Samuel Emerson, Dominic Nistal, David J. Coté et al.
1 citations
Neurosurgery
Pituitary Gland Disorders and Treatments
1.29
article

Surgical Outcomes of Silent ACTH+ Corticotroph Pituitary Neuroendocrine Tumors: A Multi-Institutional Experience and Review of the Literature

Jacob Ruzevick, Samuel Emerson, Dominic Nistal, David J. Coté, Evgeniya Tyrtova, Anthony J. DeSantis, Norman E. Garrett, R. Alan Failor, Robert G. Briggs, Brent E. Wisse, Luis F. Gonzalez‐Cuyar, Racheal Peterson, Gabriel Zada, Benjamin Fixman, Spencer Raub, Manuel Ferreira, Jessica Eaton, K. Mark Weaver, Thomas Hanks
article en
1 citations

Abstract

Silent corticotroph PitNETs have high rates of extrasellar growth, often limiting the ability to achieve gross total resection. Recurrence/progression is common, occurring in 13% to 17% of cases within two years, necessitating the need for close postoperative follow-up.

NeurosurgeryVol. 97(5)
University of Southern California (US), University of Washington (US), Neurological Surgery (US)
No poverty
Openalex Percentile: Top 20%
Pituitary Gland Disorders and Treatments
1.29
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