A case of adrenal oncocytoma: reviewing the literature of radiological finding

Oncocytoma is a tumour that predominantly occurs in the kidneys and salivary glands. Only approximately 200 cases have been reported to be of adrenal origin to date, and only a few reports about its radiological findings have been published so far. Herein, we present the CT and MRI findings of an adrenal oncocytoma observed in a patient suspected of having mitochondrial abnormalities, along with the pathological findings. The tumour was roughly classified into three areas: a hypercellular region, a region containing fibrous tissue, and an oedematous region. These corresponded to the restricted diffusion area on the apparent diffusion coefficient map, the gradually enhanced area at the secretory phase on contrast-enhanced CT scan, and the obvious hyperintensity on the T2-weighted image, respectively. We also discuss these findings in the context of previously reported radiological findings in the literature. Diagnosing adrenal oncocytoma through imaging is challenging, and it is crucial to consider the possibility of malignancy while making the differential diagnosis. Small-sized homogenous tumours may be hard to differentiate from lipid-poor adenomas, while larger inhomogeneous ones are hard to distinguish from adrenal cancer.

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Publication Details

Journal
BJR|case reports
Published
2024-08-30
DOI
https://doi.org/10.1093/bjrcr/uaae029
Citations
2
Primary Topic
Adrenal and Paraganglionic Tumors
Type
article
Field-Weighted Citation Impact
1.15
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article

A case of adrenal oncocytoma: reviewing the literature of radiological finding

Toshitaka Nagao, Natsuhiko Shirota, Yukari Wakabayashi, Yoshio Ohno et al.
2 citations
BJR|case reports
Adrenal and Paraganglionic Tumors
1.15
article

A case of adrenal oncocytoma: reviewing the literature of radiological finding

Toshitaka Nagao, Natsuhiko Shirota, Yukari Wakabayashi, Yoshio Ohno, Kazuhiro Saito, Aoi Suketa, M Sakano
article en
2 citations

Abstract

Oncocytoma is a tumour that predominantly occurs in the kidneys and salivary glands. Only approximately 200 cases have been reported to be of adrenal origin to date, and only a few reports about its radiological findings have been published so far. Herein, we present the CT and MRI findings of an adrenal oncocytoma observed in a patient suspected of having mitochondrial abnormalities, along with the pathological findings. The tumour was roughly classified into three areas: a hypercellular region, a region containing fibrous tissue, and an oedematous region. These corresponded to the restricted diffusion area on the apparent diffusion coefficient map, the gradually enhanced area at the secretory phase on contrast-enhanced CT scan, and the obvious hyperintensity on the T2-weighted image, respectively. We also discuss these findings in the context of previously reported radiological findings in the literature. Diagnosing adrenal oncocytoma through imaging is challenging, and it is crucial to consider the possibility of malignancy while making the differential diagnosis. Small-sized homogenous tumours may be hard to differentiate from lipid-poor adenomas, while larger inhomogeneous ones are hard to distinguish from adrenal cancer.

BJR|case reportsVol. 10(5)
Tokyo Medical University (JP)
Good health and well-being
Openalex Percentile: Top 21%
Adrenal and Paraganglionic Tumors
1.15
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