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.

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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
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article

Management of Non-Islet Cell Tumor Hypoglycemia Induced by Adrenal Cortical Carcinoma

Sadia Ali, Azucena Herrera Chancay, Jessica Abramowitz, Oksana Hamidi et al.
JCEM Case Reports
Adrenal and Paraganglionic Tumors
article

Management of Non-Islet Cell Tumor Hypoglycemia Induced by Adrenal Cortical Carcinoma

Sadia Ali, Azucena Herrera Chancay, Jessica Abramowitz, Oksana Hamidi, Yaling Tang, Liwei Jia
article en

Abstract

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.

JCEM Case ReportsVol. 3(12)
The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 48%
Adrenal and Paraganglionic Tumors
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