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April 27, 2026Radiology Case Reports0 citationsOpen Access

Ganglioneuroma with mesenteric involvement: An atypical presentation of a rare neoplasm

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CSConnor W. SmithFLFelipe Lopez-RamirezHLHuili Li

Key Points

  • This report aims to highlight an atypical case of ganglioneuroma with mesenteric involvement, underscoring diagnostic challenges.
  • Reporting the diagnostic process and surgical management of a 40-year-old female with a ganglioneuroma.
  • Emphasizing the integration of clinical, radiological, and histological findings for accurate diagnosis.
  • Describing the complete surgical resection performed with effective post-operative follow-up.
  • Histological examination confirmed the diagnosis of ganglioneuroma of mesenteric origin.
  • Complete surgical resection was achieved with no complications during recovery.
  • The patient remained free of recurrence for 15 years post-treatment.

Abstract

Ganglioneuromas are benign neoplasms of the neuroblastic tumor family, primarily arising from neural crest cells within the sympathetic nervous system. They are often asymptomatic and detected incidentally upon imaging for different conditions, commonly found in the mediastinum, retroperitoneum, and adrenal glands. This case report described the diagnosis and management of a 40-year-old female with a retroperitoneal ganglioneuroma featuring mesenteric involvement. The nonspecific imaging features and clinical presentation necessitated histological examination, which ultimately confirmed the diagnosis of a ganglioneuroma of mesenteric origin. The patient underwent complete surgical resection with an uneventful recovery and remains free of recurrence 15 years post-treatment. This case underscores the importance of integrating clinical, radiological, and histological findings to differentiate GNs from other soft tissue abdominal masses.

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Cite This Study

Smith et al. (2026) studied this question.

synapsesocial.com/papers/69eefcf4fede9185760d3ad8https://doi.org/10.1016/j.radcr.2026.04.022
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