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Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report
Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome. We herein report a rare case of TIO in a 58-year-old Chinese man who presented with a large lump in the right palm. Clinical, biochemical, and radiological assessments were performed. Laboratory examination showed severe hypophospha...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567775/ https://www.ncbi.nlm.nih.gov/pubmed/30859855 http://dx.doi.org/10.1177/0300060519833476 |
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author | Qian, Yanying Dai, Zhijuan Zhu, Cong Ruan, Luya Thapa, Saroj Wu, Chaoming |
author_facet | Qian, Yanying Dai, Zhijuan Zhu, Cong Ruan, Luya Thapa, Saroj Wu, Chaoming |
author_sort | Qian, Yanying |
collection | PubMed |
description | Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome. We herein report a rare case of TIO in a 58-year-old Chinese man who presented with a large lump in the right palm. Clinical, biochemical, and radiological assessments were performed. Laboratory examination showed severe hypophosphatemia, phosphaturia, an elevated serum alkaline phosphatase level, and an elevated serum fibroblast growth factor 23 (FGF-23) level. Dual-energy X-ray absorptiometry showed low bone mineral density. Magnetic resonance imaging revealed an irregular mass located in the right palm and abnormal findings in several metacarpal bones. During the operation, the surgeons found that the tumor had penetrated the surrounding muscles. The tumor had unique characteristics of local tissue invasion. The patient’s symptoms fully resolved and his serum phosphorus level normalized, although his serum FGF-23 level remained slightly high in the postoperative phase. Our findings suggest that in some patients with TIO, the serum phosphorus level might return to the normal range despite a relatively high postoperative serum FGF-23 level. These patients should be kept under close observation and regularly surveyed for any evidence of a residual tumor. |
format | Online Article Text |
id | pubmed-6567775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-65677752019-06-20 Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report Qian, Yanying Dai, Zhijuan Zhu, Cong Ruan, Luya Thapa, Saroj Wu, Chaoming J Int Med Res Case Reports Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome. We herein report a rare case of TIO in a 58-year-old Chinese man who presented with a large lump in the right palm. Clinical, biochemical, and radiological assessments were performed. Laboratory examination showed severe hypophosphatemia, phosphaturia, an elevated serum alkaline phosphatase level, and an elevated serum fibroblast growth factor 23 (FGF-23) level. Dual-energy X-ray absorptiometry showed low bone mineral density. Magnetic resonance imaging revealed an irregular mass located in the right palm and abnormal findings in several metacarpal bones. During the operation, the surgeons found that the tumor had penetrated the surrounding muscles. The tumor had unique characteristics of local tissue invasion. The patient’s symptoms fully resolved and his serum phosphorus level normalized, although his serum FGF-23 level remained slightly high in the postoperative phase. Our findings suggest that in some patients with TIO, the serum phosphorus level might return to the normal range despite a relatively high postoperative serum FGF-23 level. These patients should be kept under close observation and regularly surveyed for any evidence of a residual tumor. SAGE Publications 2019-03-12 2019-05 /pmc/articles/PMC6567775/ /pubmed/30859855 http://dx.doi.org/10.1177/0300060519833476 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Qian, Yanying Dai, Zhijuan Zhu, Cong Ruan, Luya Thapa, Saroj Wu, Chaoming Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
title | Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
title_full | Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
title_fullStr | Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
title_full_unstemmed | Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
title_short | Tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
title_sort | tumor-induced osteomalacia with the culprit lesion located in the palm: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567775/ https://www.ncbi.nlm.nih.gov/pubmed/30859855 http://dx.doi.org/10.1177/0300060519833476 |
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