上颌窦异位垂体促肾上腺皮质激素腺瘤:库欣综合征的罕见病因。

IF 0.7 Q4 OTORHINOLARYNGOLOGY
Turkish Archives of Otorhinolaryngology Pub Date : 2026-09-30 Epub Date: 2026-08-20 DOI:10.4274/tao.2026.2025-5-3
Georgina Wordsworth, Tuğba Karagöz, Kathryn Lonnen, Warren Bennett, Timothy Bates
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引用次数: 0

摘要

我们描述了一个罕见的病例库欣综合征引起的异位促肾上腺皮质激素(ACTH)分泌垂体腺瘤位于上颌窦和概述诊断和治疗的挑战。一名41岁女性,有8年进行性体重增加、疲劳、2型糖尿病和高血压病史,诊断为库欣综合征。下岩窦取样证实异位ACTH源。氟脱氧葡萄糖正电子发射断层扫描显示右侧上颌窦有12毫米病变,经鼻内入路成功切除。术后,皮质醇水平恢复正常,症状消失。术后患者病情持续缓解2.5年。本病例强调了在库欣综合征无鞍块患者中考虑异位acth分泌腺瘤的重要性,并强调需要进行彻底的诊断评估,以确保准确的肿瘤定位和最佳的手术处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ectopic ACTH-Secreting Pituitary Adenoma of the Maxillary Sinus: A Rare Cause of Cushing's Syndrome.

We describe a rare case of Cushing's syndrome caused by an ectopic adrenocorticotropic hormone (ACTH)-secreting pituitary adenoma located in the maxillary sinus and outline the diagnostic and therapeutic challenges. A 41-year-old woman presented with an eight-year history of progressive weight gain, fatigue, type 2 diabetes mellitus, and hypertension, leading to a diagnosis of Cushing's syndrome. Inferior petrosal sinus sampling confirmed an ectopic ACTH source. Fluorodeoxyglucose-positron emission tomography demonstrated a 12-mm lesion in the right maxillary sinus, which was successfully removed via an endonasal approach. Postoperatively, cortisol levels normalized and her symptoms resolved. The patient remains in remission 2.5 years following surgery. This case highlights the importance of considering ectopic ACTH-secreting adenomas in patients with Cushing's syndrome without a sellar mass and emphasizes the need for thorough diagnostic evaluation to ensure accurate tumor localization and optimal surgical management.

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