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.

引用

页数：5

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