Characteristics of benign adrenocortical adenomas with 18F-FDG PET accumulation

Author:

Ishiwata Kazuki12,Suzuki Sawako12,Igarashi Katsushi12,Ruike Yutaro12,Naito Kumiko12,Ishida Akiko12,Deguchi-Horiuchi Hanna12,Fujimoto Masanori12,Koide Hisashi12,Imamura Yusuke3,Sakamoto Shinichi3,Ichikawa Tomohiko3,Ikeda Jun-ichiro4,Yokote Koutaro12

Affiliation:

1. 1Department of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, Japan

2. 2Department of Diabetes, Metabolism and Endocrinology, Chiba University Hospital, Chiba, Japan

3. 3Department of Urology, Graduate School of Medicine, Chiba University, Chiba, Japan

4. 4Department of Diagnostic Pathology, Graduate School of Medicine, Chiba University, Chiba, Japan

Abstract

Introduction Although 18F-FDG PET was originally developed to evaluate benign and malignant tumors, the frequency of detection of benign adrenocortical adenomas showing FDG-PET accumulation has increased. However, the details of FDG-PET-accumulated benign adrenocortical adenomas have not been elucidated. Methods To elucidate the pathophysiology of FDG-PET-positive cortisol-producing adrenal tumors, we performed clinicopathological and genetic analyses of adrenocortical adenomas examing FDG-PET in 30 operated patients with unilateral cortisol-producing adrenal tumors (26 adrenal adenomas and 4 adrenal cancers). Results All adrenocortical carcinomas and 17/26 (65%) benign adrenocortical adenomas showed high FDG accumulation (SUVmax ≥ 3). In adrenocortical adenomas with high FDG accumulation (SUVmax ≥ 3), SUVmax showed a positive correlation with the CT Hounsfield units. A higher SUVmax showed a clear black adenoma appearance with predominantly compact cells, which exhibited high T1 and T2 signals, a lack of signal drop on out-of-phase imaging on MRI, and less accumulation on 131-I adsterol scintigraphy. Furthermore, RNA-sequencing analysis revealed significant increases in the lysosomal and autophagy pathways and metabolic pathways, including glycolysis through glucose transporter (GLUT) 1 and 3, in black adenomas with high-level FDG accumulation. Discussion A black adenoma is blackish due to lipofuscin, which accumulates as a result of damaged mitochondria or proteins that escape lysosomal degradation or autophagy. Since FDG in PET is taken up via GLUTs, alteration of the intracellular metabolic dynamics associated with mitochondrial damage in black adenomas may increase PET accumulation. Conclusion Black adrenal adenomas should be considered with adrenal tumors showing PET accumulation and low lipid contents.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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