An Unusual Case of Adrenocortical Carcinoma with Multiple Facets

被引：0
|
作者：
Tan, Jie En [1 ]
Tan, Florence Hui Sieng [1 ]
Kuan, Yueh Chien [1 ]
Chan, Pei Lin [1 ]
Yusri, Yusuf [2 ]
机构：
[1] Minist Hlth, Sarawak Gen Hosp, Dept Med, Endocrine Unit, Sarawak, Malaysia
[2] Minist Hlth, Sarawak Gen Hosp, Pathol Dept, Sarawak, Malaysia
来源：
JOURNAL OF THE ASEAN FEDERATION OF ENDOCRINE SOCIETIES | 2024年
关键词：
adrenocortical carcinoma; pheochromocytoma; urine fractionated metanephrines; CLINICAL-PRACTICE GUIDELINES; EUROPEAN-SOCIETY; DIAGNOSIS; MANAGEMENT; PHEOCHROMOCYTOMA; COLLABORATION; NETWORK;
D O I：
10.15605/jafes.039.02.16
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Adrenocortical carcinoma (ACC) is a rare malignant tumour 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, characteristic of pheochromocytoma. We report a case of a large functioning adrenal tumour with overlapping biochemical features of ACC and pheochromocytoma. Biopsy confirmed the histopathological diagnosis of metastatic ACC.
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页数：5
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