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04.09.2017 | case report

A rare case of Calot’s triangle paraganglioma

verfasst von: Alberto Oldani, Renzo Boldorini, Paolo Spina, Sergio Gentilli

Erschienen in: European Surgery | Ausgabe 5/2017

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Summary

Background

Paraganglioma is a rare type of neuroendocrine tumor with the ability of neuropeptide and catecholamine secretion. The most common locations of these neoplasms are head and neck regions, retroperitoneal para-aortic and paracaval, renal, and urinary bladder sympathetic plexuses; abdominal paragangliomas at other sites are extremely uncommon.

Case presentation

A 66-year-old male patient was admitted to our institution with a diagnosis of an infundibular pericholecystic mass. Laparoscopic cholecystectomy and pericholecystic mass radical exeresis was performed; histology achieved a diagnosis of paraganglioma located in Calot’s triangle.

Conclusion

The report shows an extremely rare case of an extra-adrenal abdominal paraganglioma, successfully managed with a laparoscopic approach.

Vorheriger Artikel Multimodality locoregional treatment strategies for bridging HCC patients before liver transplantation

Nächster Artikel A rare but life-threatening complication of aortic surgery: iliac appendiceal fistula

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Titel: A rare case of Calot’s triangle paraganglioma
verfasst von: Alberto Oldani
Renzo Boldorini
Paolo Spina
Sergio Gentilli
Publikationsdatum: 04.09.2017
Verlag: Springer Vienna
Erschienen in: European Surgery / Ausgabe 5/2017
Print ISSN: 1682-8631
Elektronische ISSN: 1682-4016
DOI: https://doi.org/10.1007/s10353-017-0488-7

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