A Rare Case of an Adrenal Ganglioneuroma Treated Laparoscopically in a Patient with Left-Sided Inferior Vena Cava.

Q4 Medicine
Journal of Endourology Case Reports Pub Date : 2020-12-29 eCollection Date: 2020-01-01 DOI:10.1089/cren.2020.0174
João Rafael Silva Simões Estrela, Alexandre A Ziomkowski, Frederico Mascarenhas, André Costa Matos
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引用次数: 3

Abstract

Background: Ganglioneuroma is a rare tumor derived from the neural crest that can occur in any sympathetic tissue. It corresponds to 0.3% to 2% of incidental adrenal tumors and <250 have been reported in the literature so far. Case Presentation: We present a case of a 30-year-old Caucasian woman presented with a large bilobed adrenal tumor found on a CT scan during the investigation of acute abdominal pain. The image also showed a rare anatomic variation of a left-sided inferior vena cava. Biochemical work-up for adrenal incidentaloma showed normal markers. Since we could not rule out malignancy, the patient was subjected to laparoscopic adrenalectomy and the pathology report showed an adrenal ganglioneuroma, a rare nonfunctioning tumor of the adrenal. Conclusion: Ganglioneuroma can present as a large bilobed adrenal tumor. The laparoscopic approach is feasible and safe. Preoperative planning is needed and vascular variations can be challenging during the procedure.

腹腔镜治疗左侧下腔静脉少见肾上腺神经节神经瘤1例。
背景:神经节神经瘤是一种罕见的源自神经嵴的肿瘤,可发生于任何交感神经组织。它对应于0.3%至2%的偶发肾上腺肿瘤和病例介绍:我们报告一例30岁的高加索女性,在急性腹痛的CT扫描中发现一个大的双叶肾上腺肿瘤。图像也显示了一个罕见的解剖变异左侧下腔静脉。肾上腺偶发瘤生化检查指标正常。由于不能排除恶性肿瘤,我们对患者进行了腹腔镜肾上腺切除术,病理报告显示为肾上腺神经节神经瘤,这是一种罕见的肾上腺无功能肿瘤。结论:神经节神经瘤可表现为大的双叶肾上腺肿瘤。腹腔镜入路可行且安全。术前计划是必要的,在手术过程中血管变异可能具有挑战性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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