Management of Non-Islet Cell Tumor Hypoglycemia Induced by Adrenal Cortical Carcinoma
Non-islet cell tumor hypoglycemia (NICTH) is a rare paraneoplastic syndrome that significantly worsens the prognosis of underlying malignancies. It is characterized by hypoglycemia resulting from ectopic production of insulin-like growth factor 2. NICTH caused by adrenal cortical carcinoma (ACC) is extremely rare. To date, no curative treatment of nonoperable NICTH has been reported. In this report, we describe a case of ACC-induced NICTH that was refractory to multiple treatments for hypoglycemia. It provides diagnostic and treatment approaches for NICTH and emphasizes the limitations of existing medical therapies for NICTH.
Authors
- Sadia Ali (ORCID: https://orcid.org/0000-0003-4458-7811)
- Azucena Herrera Chancay
- Jessica Abramowitz (ORCID: https://orcid.org/0000-0002-0391-7207)
- Oksana Hamidi (ORCID: https://orcid.org/0000-0002-7367-3885)
- Yaling Tang (ORCID: https://orcid.org/0000-0002-2405-2855)
- Liwei Jia (ORCID: https://orcid.org/0000-0002-2118-6428)
Institutions
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- JCEM Case Reports
- Published
- 2025-10-27
- DOI
- https://doi.org/10.1210/jcemcr/luaf245
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00