Korean J Endocr Surg.  2014 Dec;14(4):228-234. 10.0000/kaes.2014.14.4.228.

Surgical Approach of the Rare Benign Adrenal Tumor

Affiliations
  • 1Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. jinnee.kim@samsung.com

Abstract

PURPOSE
Benign adrenal tumors other than hyper-functioning tumor and non-functioning cortical adenoma are extremely rare. The purpose of this study is to review the clinical features of these rare benign adrenal tumors and to analyze their prevalence and the proper surgical approach for them.
METHODS
Among patients who underwent adrenalectomy in Samsung Medical Center, between 1997 and 2013, patients with benign adrenal tumor except non-functioning cortical adenoma, malignancy, and hyper-functioning tumor such as pheochromocytoma, aldosteronoma, and cortisol producing tumor were included. Clinical details, radiologic findings and pathologic findings as well as data associated with the surgical procedure were analyzed retrospectively.
RESULTS
The percentage of these tumors among 703 surgically removed adrenal tumors was 10.7% (75 cases). They included 30 adrenal cysts, 18 ganglioneuromas, 11 myelolipomas, seven schwannomas, and the other six were rare adrenal tumors. Approximately 40% of the patients were operated under a diagnosis different from original tumors. Operation time and hospital stay of patients who underwent laparoscopic adrenalectomy were shorter than those of patients who underwent open adrenalectomy.
CONCLUSION
These benign adrenal tumors are very rare and difficult to diagnose preoperatively. For the surgical treatment of these tumors, laparoscopic adrenalectomy is more preferable to conventional open adrenalectomy.

Keyword

Rare benign adrenal tumor; Adrenal cyst; Ganglioneuroma; Myelolipoma; Schwannoma

MeSH Terms

Adenoma
Adrenalectomy
Diagnosis
Ganglioneuroma
Humans
Hydrocortisone
Length of Stay
Myelolipoma
Neurilemmoma
Pheochromocytoma
Prevalence
Retrospective Studies
Hydrocortisone

Reference

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