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Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23
PURPOSE: Tumor-induced osteomalacia (TIO) is characterized by hypophosphatemia caused by a phosphaturic mesenchymal tumor. While surgical resection of the tumor leads to a cure, identification of the responsible tumor is challenging. Recently, several studies showed that systemic sampling of fibrobl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552653/ https://www.ncbi.nlm.nih.gov/pubmed/28792142 http://dx.doi.org/10.3349/ymj.2017.58.5.981 |
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author | Lee, Ji-Yeon Park, Hye-Sun Han, Seunghee Lim, Jiyu Kelly Hong, Namki Park, Sung Il Rhee, Yumie |
author_facet | Lee, Ji-Yeon Park, Hye-Sun Han, Seunghee Lim, Jiyu Kelly Hong, Namki Park, Sung Il Rhee, Yumie |
author_sort | Lee, Ji-Yeon |
collection | PubMed |
description | PURPOSE: Tumor-induced osteomalacia (TIO) is characterized by hypophosphatemia caused by a phosphaturic mesenchymal tumor. While surgical resection of the tumor leads to a cure, identification of the responsible tumor is challenging. Recently, several studies showed that systemic sampling of fibroblast growth factor 23 (FGF23) is helpful for localization of tumors. The present study aimed to evaluate the clinical utility of this method in Korean patients. MATERIALS AND METHODS: Six patients compatible with TIO who were admitted to our hospital between 2006 and 2015 were analyzed. Systemic venous sampling of FGF23 was performed to detect blind lesions or to confirm a suspicious lesion identified in previous imaging studies. RESULTS: Venous sampling helped confirming the tumor in five of the six patients. Three patients underwent surgery after sampling, and in two patients, the lesions were detected after 3 years by means of (68)Ga-DOTATOC positron emission tomography with computed tomography. In one patient, there was a local elevation of serum FGF23 without any related lesion on additional imaging. CONCLUSION: Our data strengthened the value of venous sampling of FGF23 in predicting the location of tumors and suggested that it can be more effective in the presence of the relevant lesion in subsequent imaging analyses. |
format | Online Article Text |
id | pubmed-5552653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-55526532017-09-01 Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 Lee, Ji-Yeon Park, Hye-Sun Han, Seunghee Lim, Jiyu Kelly Hong, Namki Park, Sung Il Rhee, Yumie Yonsei Med J Original Article PURPOSE: Tumor-induced osteomalacia (TIO) is characterized by hypophosphatemia caused by a phosphaturic mesenchymal tumor. While surgical resection of the tumor leads to a cure, identification of the responsible tumor is challenging. Recently, several studies showed that systemic sampling of fibroblast growth factor 23 (FGF23) is helpful for localization of tumors. The present study aimed to evaluate the clinical utility of this method in Korean patients. MATERIALS AND METHODS: Six patients compatible with TIO who were admitted to our hospital between 2006 and 2015 were analyzed. Systemic venous sampling of FGF23 was performed to detect blind lesions or to confirm a suspicious lesion identified in previous imaging studies. RESULTS: Venous sampling helped confirming the tumor in five of the six patients. Three patients underwent surgery after sampling, and in two patients, the lesions were detected after 3 years by means of (68)Ga-DOTATOC positron emission tomography with computed tomography. In one patient, there was a local elevation of serum FGF23 without any related lesion on additional imaging. CONCLUSION: Our data strengthened the value of venous sampling of FGF23 in predicting the location of tumors and suggested that it can be more effective in the presence of the relevant lesion in subsequent imaging analyses. Yonsei University College of Medicine 2017-09-01 2017-07-31 /pmc/articles/PMC5552653/ /pubmed/28792142 http://dx.doi.org/10.3349/ymj.2017.58.5.981 Text en © Copyright: Yonsei University College of Medicine 2017 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Ji-Yeon Park, Hye-Sun Han, Seunghee Lim, Jiyu Kelly Hong, Namki Park, Sung Il Rhee, Yumie Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 |
title | Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 |
title_full | Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 |
title_fullStr | Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 |
title_full_unstemmed | Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 |
title_short | Localization of Oncogenic Osteomalacia by Systemic Venous Sampling of Fibroblast Growth Factor 23 |
title_sort | localization of oncogenic osteomalacia by systemic venous sampling of fibroblast growth factor 23 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552653/ https://www.ncbi.nlm.nih.gov/pubmed/28792142 http://dx.doi.org/10.3349/ymj.2017.58.5.981 |
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