ACTH-producing thymic neuroendocrine tumor initially presenting as psychosis: A case report and literature review.

Taiki Okumura, Shohei Takayama, Shin-Ichi Nishio, Takahiro Miyakoshi, Takuro Noguchi, Takashi Kobayashi, Toshirou Fukushima, Nodoka Sekiguchi, Toshiaki Otsuki, Mitsuhisa Komatsu, Tomonobu Koizumi

Journal: Thoracic cancer 2020;10(7):1648-1653

PMID: 31187563

Abstract

A 32-year-old woman was referred to our hospital because of severe psychosis and was found to have an ectopic ACTH-producing thymic neuroendocrine tumor. Laboratory data revealed an elevated serum cortisol and plasma ACTH level, hypokalemia, and metabolic alkalosis. Chest computed tomography (CT) revealed an anterior mediastinal mass and multiple pulmonary nodules. As the patient was unable to communicate because of her consciousness disturbance, she was managed with artificial ventilation and deep sedation. Metyrapone and potassium supplementation were administered, and steroid psychosis gradually improved. Thoracic surgery was performed and the histopathological diagnosis was thymic neuroendocrine tumor with positive anti-ACTH immunohistochemical staining. Here we present details of the case and review the literature.

© 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.

Address: Second Department of Internal Medicine, Shinshu University School of Medicine, Asahi Matsumoto, Japan.; Department of Comprehensive Cancer Therapy, Shinshu University School of Medicine, Asahi Matsumoto, Japan.; Fourth Department of Internal Medicine, Shinshu University School of Medicine, Asahi Matsumoto, Japan.; Department of Central Laboratory, Shinshu University School of Medicine, Asahi Matsumoto, Japan.
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.