Management of an ACTH Secreting Pituitary Adenoma Causing Persistent Cushing's Disease: Management of Residual Cavernous Sinus Invasion

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Authors: Jonathan Balquiedra Lamano, Erik Sosa, Matei A. Banu, Lirit Levi, Peter H. Hwang, Juan Carlos Fernandez-Miranda
Cited by: 0

Abstract

The case of a 32-year-old female with persistent hypercortisolism and Cushing’s disease due to residual tumor within the cavernous sinus demonstrates the importance of the resection of cavernous sinus disease for obtaining biochemical remission. On repeat endoscopic endonasal resection, tumor was found to be involving the medial wall of the cavernous sinus, inferior compartment of the cavernous sinus, and invading the carotid clinoidal ligaments. Resection of this residual tumor resulted in immediate biochemical remission. Publication History Article published online: 27 February 2026 © 2026. Thieme. All rights reserved. Georg Thieme Verlag KG Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

Fields of Study & Subjects

Pituitary Gland Disorders and Treatments Head and Neck Surgical Oncology Meningioma and schwannoma management

Publication details

Journal / source
Journal of Neurological Surgery Part B Skull Base
Volume
87
Issue
S 01
Pages
S1–S548
Publication date
27 February 2026
Language
EN