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表现为肾上腺偶发瘤的神经节瘤:保留肾上腺手术的可行性

Ganglioneuroma presenting as an adrenal incidentaloma: Feasibility of adrenal-sparing surgery.

作者信息

Ranjan Rohit, Mittal Ankur, Ranjan Satish Kumar, Panwar Vikas, Talwar Harkirat Singh

机构信息

Department of Urology, All India Institute of Medical Science, Rishikesh, Uttarakhand, India.

出版信息

J Minim Access Surg. 2021 Jul-Sep;17(3):389-391. doi: 10.4103/jmas.JMAS_147_20.

Abstract

Adrenal ganglioneuromas (GNs) are very rare tumours that originate from neural crest cells. Most of the time, they are diagnosed incidentally as they are usually non-functional and remain asymptomatic. Nowadays, they are being detected more often due to better availability of imaging facilities such as computed tomography (CT)/magnetic resonance imaging (MRI). Minimally invasive adrenalectomy (laparoscopic or robotic) remains the standard of care for such lesions. Hereby, we report a case of a 15-year-old young girl with right adrenal incidentaloma which was diagnosed on CT with the features suggestive of GN. She underwent robot-assisted excision of the mass with adrenal-sparing surgery. Histopathology revealed benign GN and no adjuvant treatment was required. As GN is not known for recurrence or metastasis, minimal invasive adrenal-sparing surgery should be a preferred modality of choice.

摘要

肾上腺神经节细胞瘤(GNs)是非常罕见的起源于神经嵴细胞的肿瘤。大多数情况下,它们是在偶然情况下被诊断出来的,因为它们通常无功能且无症状。如今,由于诸如计算机断层扫描(CT)/磁共振成像(MRI)等成像设备的更广泛应用,它们被发现的频率更高。微创肾上腺切除术(腹腔镜或机器人辅助)仍然是这类病变的标准治疗方法。在此,我们报告一例15岁年轻女孩,其右肾上腺意外瘤在CT上被诊断出具有提示GN的特征。她接受了机器人辅助的肿物切除并保留肾上腺手术。组织病理学显示为良性GN,无需辅助治疗。由于GN不会复发或转移,微创保留肾上腺手术应是首选的治疗方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b574/8270040/3f7816bf45e2/JMAS-17-389-g001.jpg

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本文引用的文献

1
Laparoscopic adrenalectomy for ganglioneuroma presenting as an adrenal incidentaloma.
J Minim Access Surg. 2019 Jul-Sep;15(3):259-261. doi: 10.4103/jmas.JMAS_228_18.
2
Adrenal ganglioneuroma: What you need to know.
World J Clin Cases. 2017 Oct 16;5(10):373-377. doi: 10.12998/wjcc.v5.i10.373.
3
Imaging Features of Various Adrenal Neoplastic Lesions on Radiologic and Nuclear Medicine Imaging.
AJR Am J Roentgenol. 2015 Sep;205(3):554-63. doi: 10.2214/AJR.15.14467.
4
Ganglioneuroma of the adrenal gland and retroperitoneum: A case report.
N Am J Med Sci. 2011 Jul;3(7):336-8. doi: 10.4297/najms.2011.3336.

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