A case of adrenocortical carcinoma accompanying secondary acute adrenal hypofunction postoperation

3Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background: Adrenocortical carcinoma (ACC) is a rare, heterogeneous malignancy with a poor prognosis. ACCs are classified as functioning and non-functioning. The pathogenesis of ACC remains elusive, and diagnosis of ACC is currently based on pathology. In the absence of other effective approaches, surgical resection is the preferred treatment option. Case presentation: Here, we report a case of ACC in the retroperitoneum. The patient underwent radical adrenalectomy and remained disease-free throughout a 6-month follow-up. Conclusions: Radical surgical resection is an efficient therapy for ACC, and hydrocortisone can be used to alleviate symptoms of secondary acute adrenal hypofunction.

Cite

CITATION STYLE

APA

Kou, K., Zhang, H., Zhang, C., Xie, E., Chen, Y., Wang, G., & Lv, G. (2018). A case of adrenocortical carcinoma accompanying secondary acute adrenal hypofunction postoperation. World Journal of Surgical Oncology, 16(1). https://doi.org/10.1186/s12957-018-1326-5

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free