Case Report of a Rare Tumor in the Greater Omentum
Author Information
Author(s): Archontovasilis Fotios, Markogiannakis Haridimos, Dikoglou Christina, Drimousis Panagiotis, Toutouzas Konstantinos G, Theodorou Dimitrios, Katsaragakis Stilianos
Primary Institution: Hippokrateion Hospital, Athens Medical School, University of Athens
Hypothesis
The paraganglioma in our patient was derived from the paraganglionic cells by vertebral migration from the root of the superior mesenteric artery.
Conclusion
This case highlights the rarity of paraganglioma in the greater omentum and emphasizes the importance of thorough histopathologic evaluation for diagnosis.
Supporting Evidence
- This is the second reported case of greater omentum paraganglioma.
- The tumor was completely excised and the patient remains free of disease for 2 years.
- Histopathologic evaluation is imperative for diagnosis.
Takeaway
A woman found to have a rare tumor in her abdomen was treated successfully, and she has been healthy for two years after surgery.
Methodology
The tumor was diagnosed through imaging and histopathologic evaluation, followed by surgical excision.
Limitations
The rarity of the tumor makes it difficult to establish clear diagnostic criteria for malignancy.
Participant Demographics
46-year-old woman with an unremarkable medical history.
Digital Object Identifier (DOI)
Want to read the original?
Access the complete publication on the publisher's website