| Literature DB >> 20412663 |
Miguel Angel Arrabal-Polo1, Miguel Arrabal-Martin, Victor Manuel Lopez-Leon, Felix Abad-Menor, Francisco Valle-Diaz de la Guardia, Jose Luis Mijan-Ortiz, Armando Zuluaga-Gomez.
Abstract
We demonstrate a novel clinical presentation of paraganglioma not described in the literature. The paraganglioma is a catecholamine secretory, or non-secretory, neuroendocrine tumour that derives from chromaffin cells. Its frequency, with regard to pheochromocytoma, is low, and the abdominal region is the most frequent localisation site, followed in importance by the cervical region. We report the case of a 54-year-old woman diagnosed with a retroperitoneal abscess; after drainage of the lesion, samples indicated necrotic paraganglioma cells, so it was decided to conduct a survey to determine catecholamine levels in urine, and carry out a MIBG gammagraphy, which described a non-functioning retroperitoneal paraganglioma that underwent surgical removal. There was no residual disease after 3-month follow-up.Entities:
Mesh:
Year: 2010 PMID: 20412663 PMCID: PMC5696811 DOI: 10.1308/147870810X12659688851555
Source DB: PubMed Journal: Ann R Coll Surg Engl ISSN: 0035-8843 Impact factor: 1.891