A rare case of Calot’s triangle paraganglioma

Alberto Oldani, Renzo Boldorini, Paolo Spina, Sergio Gentilli

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

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.

Lingua originaleInglese
pagine (da-a)244-247
Numero di pagine4
RivistaEuropean Surgery - Acta Chirurgica Austriaca
Volume49
Numero di pubblicazione5
DOI
Stato di pubblicazionePubblicato - 1 ott 2017

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