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Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity

Objectives Oncogenic osteomalacia is a paraneoplastic syndrome in which the tumor secretes a peptide-like hormone, fibroblast growth factor, resulting in urinary loss of phosphates. Methods We present the case of a 50-year-old woman with a benign phosphaturic mesenchymal tumor (PMT) involving the et...

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Detalles Bibliográficos
Autores principales: Arnaoutakis, Demetri, Naseri, Iman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648724/
https://www.ncbi.nlm.nih.gov/pubmed/26623233
http://dx.doi.org/10.1055/s-0035-1562852
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author Arnaoutakis, Demetri
Naseri, Iman
author_facet Arnaoutakis, Demetri
Naseri, Iman
author_sort Arnaoutakis, Demetri
collection PubMed
description Objectives Oncogenic osteomalacia is a paraneoplastic syndrome in which the tumor secretes a peptide-like hormone, fibroblast growth factor, resulting in urinary loss of phosphates. Methods We present the case of a 50-year-old woman with a benign phosphaturic mesenchymal tumor (PMT) involving the ethmoid sinus with obstruction of the ostiomeatal complex causing unilateral nasal airway obstruction. Results The tumor was initially thought to be an esthesioneuroblastoma based on primary pathology interpretation and on clinical and radiographic appearance. However, a benign PMT was later confirmed by further testing. Conclusion The tumor was removed entirely by the endoscopic transnasal approach, leading to a full resolution of symptoms.
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spelling pubmed-46487242015-11-30 Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity Arnaoutakis, Demetri Naseri, Iman J Neurol Surg Rep Article Objectives Oncogenic osteomalacia is a paraneoplastic syndrome in which the tumor secretes a peptide-like hormone, fibroblast growth factor, resulting in urinary loss of phosphates. Methods We present the case of a 50-year-old woman with a benign phosphaturic mesenchymal tumor (PMT) involving the ethmoid sinus with obstruction of the ostiomeatal complex causing unilateral nasal airway obstruction. Results The tumor was initially thought to be an esthesioneuroblastoma based on primary pathology interpretation and on clinical and radiographic appearance. However, a benign PMT was later confirmed by further testing. Conclusion The tumor was removed entirely by the endoscopic transnasal approach, leading to a full resolution of symptoms. Georg Thieme Verlag KG 2015-08-21 2015-11 /pmc/articles/PMC4648724/ /pubmed/26623233 http://dx.doi.org/10.1055/s-0035-1562852 Text en © Thieme Medical Publishers
spellingShingle Article
Arnaoutakis, Demetri
Naseri, Iman
Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity
title Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity
title_full Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity
title_fullStr Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity
title_full_unstemmed Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity
title_short Sinonasal Phosphaturic Mesenchymal Tumor: A Rare and Misinterpreted Entity
title_sort sinonasal phosphaturic mesenchymal tumor: a rare and misinterpreted entity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648724/
https://www.ncbi.nlm.nih.gov/pubmed/26623233
http://dx.doi.org/10.1055/s-0035-1562852
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