Literature DB >> 16824474

[Surgical management of a preaortic paraganglioma: Report of one case].

P Puche1, E Jacquet, P-E Colombo, S Jaber, P Alric, J-P Carabalona, H Bouyabrine, J Domergue, F Navarro.   

Abstract

Paragangliomas (PG) are rare and often diagnosed in the young adult. One case of retroperitoneal preaortic paraganglioma localised between the celiac trunk and the superior mesenteric artery is reported. The management of paraganglioma involves endocrinologists, geneticists and surgeons but the only potentially curative treatment remains surgical resection. Pathology reports can not always discriminate between benign or malignant tumors. Hereditary in paraganglioma occurs in approximately 25% of cases. Genetic investigation is therefore mandatory in all patients with PG. Since the type of genetic mutation is correlated with tumoral aggressiveness, genetic investigation results should be taken into account when a surgical procedure is planned.

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Year:  2006        PMID: 16824474     DOI: 10.1016/j.anchir.2006.05.005

Source DB:  PubMed          Journal:  Ann Chir        ISSN: 0003-3944


  3 in total

1.  Retroperitoneal paragangliomas: Report of 4 cases.

Authors:  Helmi Kallel; Hassen Hentati; Amine Baklouti; Ali Gassara; Ahmed Saadaoui; Ghassen Halek; Sana Landolsi; Ma El Ouaer; Wajdi Chaieb; Fethia Maamouri; Saber Mannaï
Journal:  World J Gastrointest Surg       Date:  2014-04-27

2.  [Retroperitoneal non-secreting paraganglioma: a rare cause of high intestinal occlusion].

Authors:  Mehdi Soufi; Said Benamr; Bouziane Chad
Journal:  Pan Afr Med J       Date:  2014-08-20

3.  [Perioperative management of a retroperitoneal paraganglioma].

Authors:  Amine Bouslama; Jaballah Sakhri; Hamdi Echehoumi; Afraa Brahim; Fehmi Ferhi; Dhafer Ben Létaifa
Journal:  Pan Afr Med J       Date:  2015-08-26
  3 in total

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