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

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.

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Publication Details

Journal
Case Reports in Medicine
Published
2025-01-01
DOI
https://doi.org/10.1155/carm/7440806
Citations
1
Primary Topic
Adrenal and Paraganglionic Tumors
Type
article
Field-Weighted Citation Impact
2.01
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article

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

Abdolreza Mohammadi, Seyed Mohammad Kazem Aghamir, Fardin Asgari, M Rezayat et al.
1 citations
Case Reports in Medicine
Adrenal and Paraganglionic Tumors
2.01
article

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

Abdolreza Mohammadi, Seyed Mohammad Kazem Aghamir, Fardin Asgari, M Rezayat, Ehsan Zemanati Yar, Mahdi Najarzadegan
article en
1 citations

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.

Case Reports in MedicineVol. 2025(1)
Tehran University of Medical Sciences (IR)
Openalex Percentile: Top 18%
Adrenal and Paraganglionic Tumors
2.01
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Synchronous Ipsilateral Adrenal and Retroperitoneal Ganglioneuroma: A Unique Case of Large Tumor Mass — Abdolreza Mohammadi, Seyed Mohammad Kazem Aghamir, et al. · Case Reports in Medicine (2025) | TGRS Research Map | TGRS