Literature DB >> 25817505

A rare abdomino-pelvic tumor: paraganglioma.

Célia Pedroso1, Raquel Robalo, Pedro Sereno, Carlos Barros, Carlos Marques.   

Abstract

Paragangliomas are rare tumors, with a reported incidence of 2-8 per million. They are chromaffin cell tumors that develop from the neural crest cells and may be divided in tumors derived from the parasympathetic or sympathetic ganglia. We report a case a of a 32-year-old nulliparous woman, referred to our Infertility Clinic. Abdomino-pelvic ultrasound identified a large abdominopelvic tumor, without ovarian origin (both ovaries were identified and had normal morphology). Magnetic Resonance Imaging suggested a right adnexal multicystic, vascularized mass close to iliac vessels and questioning an ovarian origin. At exploratory laparotomy, a 10 cm encapsulated and vascularized mass was found beginning just below right renal artery and extending to the level of the broad ligament. This mass was totally excised and histopathology was consistent with Paraganglioma.

Entities:  

Mesh:

Year:  2015        PMID: 25817505     DOI: 10.20344/amp.5403

Source DB:  PubMed          Journal:  Acta Med Port        ISSN: 0870-399X


  1 in total

1.  Trauma-Induced Retroperitoneal Paraganglioma Rupture Which Was Misunderstood as a Massive Retroperitoneal Hemorrhage.

Authors:  Hongjin Shim; Ji Young Jang; Yeong Ju Kim; Jung Soo Lim; Keum Seok Bae
Journal:  Acute Crit Care       Date:  2018-04-26
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.