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A Rare Abdomino-Pelvic Tumor: Paraganglioma

dc.contributor.authorPedroso, C
dc.contributor.authorRobalo, R
dc.contributor.authorSereno, P
dc.contributor.authorBarros, C
dc.contributor.authorMarques, C
dc.date.accessioned2015-03-04T17:38:49Z
dc.date.available2015-03-04T17:38:49Z
dc.date.issued2015
dc.description.abstractParagangliomas 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.por
dc.identifier.citationActa Med Port 2015 Jan-Feb; 28 (1): 114-116por
dc.identifier.urihttp://hdl.handle.net/10400.17/2030
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherCentro Editor e Livreiro da Ordem dos Médicospor
dc.subjectMAC GINpor
dc.subjectAbdominal Neoplasms/diagnosispor
dc.subjectAbdominal Neoplasms/surgerypor
dc.subjectParaganglioma/diagnosispor
dc.subjectParaganglioma/surgery
dc.subjectPelvic Neoplasms/diagnosis
dc.subjectPelvic Neoplasms/surgery
dc.titleA Rare Abdomino-Pelvic Tumor: Paragangliomapor
dc.title.alternativeUm Caso Raro de Tumor Abdominopélvico: Paragangliomapor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage116por
oaire.citation.startPage114por
oaire.citation.titleActa Médica Portuguesapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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