Adrenocortical tumors in children 18 years old and younger.
10.4174/jkss.2012.82.4.246
- Author:
Min Jeng CHO
1
;
Dae Yeon KIM
;
Seong Chul KIM
;
Tae Hoon KIM
;
In Koo KIM
Author Information
1. Division of Pediatric Surgery, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. kimdy@amc.seoul.kr
- Publication Type:Original Article
- Keywords:
Adrenocortical adenoma;
Carcinoma;
Child
- MeSH:
Adenoma;
Adrenalectomy;
Adrenocortical Adenoma;
Child;
Cushing Syndrome;
Follow-Up Studies;
Hematuria;
Humans;
Hyperaldosteronism;
Prognosis;
Recurrence;
Retrospective Studies;
Tumor Burden;
Virilism
- From:Journal of the Korean Surgical Society
2012;82(4):246-250
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Pediatric adrenocortical tumors (ACTs) are rare. We reviewed findings in 8 children, 18 years of age or younger, diagnosed with ACT in our institution over the past 15 years. METHODS: We retrospectively reviewed 8 children with ACTs treated between 1996 and 2010. RESULTS: Three girls and 5 boys were treated for ACTs; their median age at presentation was 144 months (range, 28 months to 18 years). Seven patients showed signs of endocrine dysfunction, 4 with Cushing syndrome, 2 with virilization, and 1 with hyperaldosteronism. One patient, with symptoms of hematuria, underwent a computed tomography scan, which showed an adrenal mass. The median duration of symptoms prior to resection was 6 months (range, 1 to 24 months). Five patients had adenomas and 3 had carcinomas. All underwent complete resection of the tumor, with laparoscopic adrenalectomy performed on 3 patients with adenoma and 1 with carcinoma. The median tumor weight was 12.5 g (range, 1 to 130 g) and the median tumor volume was 18.3 cm3 (range, 2.2 to 299.2 cm3). At a median follow-up of 5.1 years (range, 4 months to 15 years), all 8 patients remain alive with no recurrence of disease. CONCLUSION: The characteristics of pediatric ACTs vary considerably. Laboratory findings, clinical hormonal features, and tumor size could not distinguish adenomas from carcinomas before surgery. Complete tumor resection was successful, with no tumor recurrence. However, the small number of patients and short follow-up period limit assessments of prognosis.
