This report describes the first known case of sarcoma arising in oncocytic adrenal cortical carcinoma, highlighting its aggressive nature and rapid progression.
Answers are grounded in this paper and cite their sources.
Signals aggressive course with rapid metastases and death; extends adrenal carcinoma spectrum but leaves management undefined.
Adrenal cortical carcinosarcoma is a rare variant of adrenal cortical carcinoma. Sarcomatous change in adrenal cortical carcinomas is exceptionally rare, with only 9 cases previously described. Adrenal cortical carcinosarcomas tend to be aggressive tumors, with locoregional recurrence and rapid metastases from the sarcomatoid component. We describe what seems to be the first case of sarcoma arising in oncocytic adrenal cortical carcinoma. The sarcomatous component here was pleomorphic rhabdomyosarcoma. This occurred in a 45-year-old man who had nodal and pulmonary metastases of the rhabdomyosarcomatous component at presentation and who died of progressive disease 11 months later. Here, we discuss the clinical, radiologic, and pathologic findings and review the literature on adrenal cortical carcinosarcomas.
No takes yet. Share an insight, caveat, or question.
Thway et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: