Surgical management of pancreatic ganglioneuroma in a child: case report.

IF 0.5 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2026-05-03 eCollection Date: 2026-05-01 DOI:10.1093/jscr/rjag341
João Victor Risso, Carmem Maria Costa Mendonça Fiori, Gabriel da Rocha Bonatto, Matheus Takahashi Garcia, Carlos Floriano de Morais
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引用次数: 0

Abstract

This report describes an exceptional paediatric case of a ganglioneuroma arising in the pancreatic topography, a rare condition that may mimic more aggressive neoplasms and hinder appropriate management selection. A previously healthy 7-year-old girl presented with a non-specific acute febrile syndrome, prompting an expanded diagnostic evaluation. Imaging studies revealed a well-defined solid mass adjacent to the pancreatic head, accompanied by minimal and non-contributory laboratory abnormalities. Given the persistent aetiological uncertainty and the intimate relationship of the lesion with major vascular structures, a surgical approach was indicated. Intraoperative histopathological assessment confirmed the diagnosis of ganglioneuroma, enabling conservative resection with adequate anatomical preservation. The postoperative course was uneventful, culminating in satisfactory recovery. This case highlights the importance of a structured multidisciplinary approach for guiding precise decision-making in the management of paediatric pancreatic masses.

儿童胰神经节神经瘤的手术治疗:1例报告。
本报告描述了一个特殊的儿童病例神经节神经瘤出现在胰腺地形,一种罕见的条件,可能模仿更积极的肿瘤和阻碍适当的管理选择。先前健康的7岁女孩表现为非特异性急性发热综合征,促使扩大诊断评估。影像学检查显示胰头附近有一界限明确的实性肿块,伴少量非辅助性实验室异常。鉴于持续的病因不确定和病变与主要血管结构的密切关系,建议手术入路。术中组织病理学评估证实了神经节神经瘤的诊断,允许保守切除并保留足够的解剖结构。术后过程平淡无奇,最终恢复满意。本病例强调了结构化多学科方法在指导儿科胰腺肿块管理中精确决策的重要性。
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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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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