Synchronous Ipsilateral Adrenal and Retroperitoneal Ganglioneuroma: A Unique Case of Large Tumor Mass.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL Case Reports in Medicine Pub Date : 2025-03-25 eCollection Date: 2025-01-01 DOI:10.1155/carm/7440806
Abdolreza Mohammadi, Fardin Asgari, Ehsan Zemanati Yar, Mina Rezayat, Mahdi Najarzadegan, Seyed Mohammad Kazem Aghamir
{"title":"Synchronous Ipsilateral Adrenal and Retroperitoneal Ganglioneuroma: A Unique Case of Large Tumor Mass.","authors":"Abdolreza Mohammadi, Fardin Asgari, Ehsan Zemanati Yar, Mina Rezayat, Mahdi Najarzadegan, Seyed Mohammad Kazem Aghamir","doi":"10.1155/carm/7440806","DOIUrl":null,"url":null,"abstract":"<p><p>This case report presents a rare instance of synchronous adrenal ganglioneuroma and an ipsilateral retroperitoneal mass in a 51-year-old woman with episodic hypertensive crises and increased symptom frequency. Imaging revealed a hypodense mass near the right kidney and an additional adrenal mass, which led to surgical intervention. Laboratory findings indicated hypercortisolism, and both masses were surgically removed by the laparoscopy approach. Postoperative pathology identified both masses as maturing-type ganglioneuroma, with no signs of malignancy or complications. This case highlights the diagnostic and therapeutic challenges of such rare presentations and emphasizes the importance of detailed imaging, surgical excision, and histopathological analysis. The potential link between elevated cortisol levels and ganglioneuroma, as observed here, underscores the need for further research into these benign tumors.</p>","PeriodicalId":9627,"journal":{"name":"Case Reports in Medicine","volume":"2025 ","pages":"7440806"},"PeriodicalIF":0.7000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11961276/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/carm/7440806","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

This case report presents a rare instance of synchronous adrenal ganglioneuroma and an ipsilateral retroperitoneal mass in a 51-year-old woman with episodic hypertensive crises and increased symptom frequency. Imaging revealed a hypodense mass near the right kidney and an additional adrenal mass, which led to surgical intervention. Laboratory findings indicated hypercortisolism, and both masses were surgically removed by the laparoscopy approach. Postoperative pathology identified both masses as maturing-type ganglioneuroma, with no signs of malignancy or complications. This case highlights the diagnostic and therapeutic challenges of such rare presentations and emphasizes the importance of detailed imaging, surgical excision, and histopathological analysis. The potential link between elevated cortisol levels and ganglioneuroma, as observed here, underscores the need for further research into these benign tumors.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
同侧肾上腺及腹膜后神经节神经瘤:一个独特的大肿瘤肿块病例。
这个病例报告了一个罕见的同步肾上腺神经节神经瘤和同侧腹膜后肿块的51岁女性发作性高血压危象和增加的症状频率。影像显示右肾附近有一个低密度肿块和一个额外的肾上腺肿块,导致手术干预。实验室结果显示高皮质醇,两个肿块通过腹腔镜手术切除。术后病理证实两个肿块为成熟型神经节神经瘤,无恶性征象或并发症。本病例强调了这种罕见表现的诊断和治疗挑战,并强调了详细成像,手术切除和组织病理学分析的重要性。正如本文所观察到的,皮质醇水平升高与神经节神经瘤之间的潜在联系强调了对这些良性肿瘤进行进一步研究的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
期刊最新文献
"White Cord Syndrome": A Reperfusion Injury Following Laminectomy and Spinal Decompression Surgery-A Case Report and Literature Review. A New Perspective on Lumbar Disc Herniation Management Using Prone Knee Extension. Management of Ablation-Refractory Atrial Fibrillation During Pregnancy. A Rare Presentation of Babesia-Associated Splenic Infarction in an Immunocompetent Young Male With Mild Parasitemia. Systemic Lupus Erythematosus and Acute Transverse Myelitis: An Unusual Association-A Case Report.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1