Clinical features and treatment options for pediatric adrenal incidentalomas: a retrospective single center study

Abstract Background The aim of this study was to investigate the clinical features and treatment options for pediatric adrenal incidentalomas(AIs) to guide the diagnosis and treatment of these tumors. Methods The clinical data of AI patients admitted to our hospital between December 2016 and Decembe...

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Main Authors: Xiaojiang Zhu (Author), Saisai Liu (Author), Yimin Yuan (Author), Nannan Gu (Author), Jintong Sha (Author), Yunfei Guo (Author), Yongji Deng (Author)
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Published: BMC, 2024-03-01T00:00:00Z.
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001 doaj_e19d2a1c0f6a46a5879664b7ba6e8f49
042 |a dc 
100 1 0 |a Xiaojiang Zhu  |e author 
700 1 0 |a Saisai Liu  |e author 
700 1 0 |a Yimin Yuan  |e author 
700 1 0 |a Nannan Gu  |e author 
700 1 0 |a Jintong Sha  |e author 
700 1 0 |a Yunfei Guo  |e author 
700 1 0 |a Yongji Deng  |e author 
245 0 0 |a Clinical features and treatment options for pediatric adrenal incidentalomas: a retrospective single center study 
260 |b BMC,   |c 2024-03-01T00:00:00Z. 
500 |a 10.1186/s12887-024-04673-7 
500 |a 1471-2431 
520 |a Abstract Background The aim of this study was to investigate the clinical features and treatment options for pediatric adrenal incidentalomas(AIs) to guide the diagnosis and treatment of these tumors. Methods The clinical data of AI patients admitted to our hospital between December 2016 and December 2022 were collected and retrospectively analyzed. All patients were divided into neonatal and nonneonatal groups according to their age at the time of the initial consultation. Results In the neonatal group, 13 patients were observed and followed up, and the masses completely disappeared in 8 patients and were significantly reduced in size in 5 patients compared with the previous findings. Four patients ultimately underwent surgery, and the postoperative pathological diagnosis was neuroblastoma in three patients and teratoma in one patient. In the nonneonatal group, there were 18 cases of benign tumors, including 9 cases of ganglioneuroma, 2 cases of adrenocortical adenoma, 2 cases of adrenal cyst, 2 cases of teratoma, 1 case of pheochromocytoma, 1 case of nerve sheath tumor, and 1 case of adrenal hemorrhage; and 20 cases of malignant tumors, including 10 cases of neuroblastoma, 9 cases of ganglioneuroblastoma, and 1 case of adrenocortical carcinoma. Conclusions Neuroblastoma is the most common type of nonneonatal AI, and detailed laboratory investigations and imaging studies are recommended for aggressive evaluation and treatment in this population. The rate of spontaneous regression of AI is high in neonates, and close observation is feasible if the tumor is small, confined to the adrenal gland and has no distant metastasis. 
546 |a EN 
690 |a Adrenal incidentaloma 
690 |a Children 
690 |a Retrospective 
690 |a Clinical analysis 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024) 
787 0 |n https://doi.org/10.1186/s12887-024-04673-7 
787 0 |n https://doaj.org/toc/1471-2431 
856 4 1 |u https://doaj.org/article/e19d2a1c0f6a46a5879664b7ba6e8f49  |z Connect to this object online.