An Unusual Case of Adrenocortical Carcinoma with Multiple Facets

A Case Report

Authors

DOI:

https://doi.org/10.15605/jafes.039.02.16

Keywords:

adrenocortical carcinoma, pheochromocytoma, urine fractionated metanephrines

Abstract

Adrenocortical carcinoma (ACC) is a rare malignant tumour originating from the adrenal cortex. Half of the cases are functional, with ACTH independent autonomous cortisol production being the most common. It is rare for ACC to present with markedly elevated metanephrine levels which is a typical characteristic of pheochromocytoma. We report a case of a large functioning adrenal tumour with overlapping biochemistry features of ACC and pheochromocytoma. Biopsy confirmed the histopathological diagnosis of metastatic ACC.  

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Author Biographies

Jie En Tan, Sarawak General Hospital

Endocrine Unit, Department Of Medicine, Sarawak General Hospital, Ministry of Health, Malaysia. Trainee.

Florence Hui Sieng Tan, Sarawak General Hospital

Endocrine Unit, Department of Medicine

Yueh Chien Kuan, Sarawak General Hospital

Endocrine Unit, Department of Medicine

Pei Lin Chan, Sarawak General Hospital

Endocrine Unit, Department of Medicine

Yusri Yusuf , Sarawak General Hospital

Pathology Department

References

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Published

2024-09-03

How to Cite

Tan, J. E., Tan, F. H. S., Kuan, Y. C., Chan, P. L., & Yusuf , Y. . (2024). An Unusual Case of Adrenocortical Carcinoma with Multiple Facets : A Case Report. Journal of the ASEAN Federation of Endocrine Societies, 39(2), 92–96. https://doi.org/10.15605/jafes.039.02.16

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Case Reports