Tumor-induced hypophosphatemia
Significant hypophosphatemia is commonly due to Vitamin D deficiency. Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such...
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| Veröffentlicht in: | Indian journal of nephrology 2017-01, Vol.27 (1), p.66-68 |
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| container_title | Indian journal of nephrology |
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| creator | Mulani, M Somani, K Bichu, S Billa, V |
| description | Significant hypophosphatemia is commonly due to Vitamin D deficiency. Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such conditions in early stages. Prompt treatment of the cause can correct this biochemical abnormality. We describe a case report of a woman presenting with severe hypophosphatemia and osteomalacia, leading eventually to the diagnosis of a phosphaturic mesenchymal tumor of the temporo-occipital bone. Surgical resection of tumor led to normalization of the biochemical parameters as well as a complete clinical recovery. |
| doi_str_mv | 10.4103/0971-4065.179302 |
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Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such conditions in early stages. Prompt treatment of the cause can correct this biochemical abnormality. We describe a case report of a woman presenting with severe hypophosphatemia and osteomalacia, leading eventually to the diagnosis of a phosphaturic mesenchymal tumor of the temporo-occipital bone. Surgical resection of tumor led to normalization of the biochemical parameters as well as a complete clinical recovery.</description><identifier>ISSN: 0971-4065</identifier><identifier>EISSN: 1998-3662</identifier><identifier>DOI: 10.4103/0971-4065.179302</identifier><identifier>PMID: 28182049</identifier><language>eng</language><publisher>India: Wolters Kluwer India Pvt. 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Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such conditions in early stages. Prompt treatment of the cause can correct this biochemical abnormality. We describe a case report of a woman presenting with severe hypophosphatemia and osteomalacia, leading eventually to the diagnosis of a phosphaturic mesenchymal tumor of the temporo-occipital bone. Surgical resection of tumor led to normalization of the biochemical parameters as well as a complete clinical recovery.</description><subject>Care and treatment</subject><subject>Case Report</subject><subject>Case studies</subject><subject>Complications and side effects</subject><subject>Diagnosis</subject><subject>Hypophosphatemia</subject><subject>Risk factors</subject><subject>Tumors</subject><issn>0971-4065</issn><issn>1998-3662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkc1r3DAQxUVpabbb3nsKhUJv3ur741IIoW0CgVzS86CV5ViJbbmSnSX_fbVssqyh6CCh-b3HzDyEPhO84QSz79goUnEsxYYowzB9g1bEGF0xKelbtDqWz9CHnB8wpoIb8R6dUU00xdys0Pnd3MdUhaGena-_tM9jHNuYx9ZOvg_2I3rX2C77Ty_3Gv359fPu8qq6uf19fXlxUzmuZK7IVltdNx4rqwz2xDFSe84xVrXRxHK9JZxSW1PjpCkP5phgyomCECuVYmv04-A7ztve184PU7IdjCn0Nj1DtAGWlSG0cB-fQFAhjOHF4OuLQYp_Z58neIhzGkrPQLSQEiulTqh723kIQxOLmetDdnBRBtFU47LWNdr8hyqnLitxcfBNKP8LwbcTQettN7U5dvMU4pCXID6ALsWck2-OExIM-0RhHxnsI4NDokVyfrqZo-A1wgLcHoBd7Caf8mM373yCwj4Ocbcwrk6MQUpYZA-v2bN_sDKykw</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Mulani, M</creator><creator>Somani, K</creator><creator>Bichu, S</creator><creator>Billa, V</creator><general>Wolters Kluwer India Pvt. 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| ispartof | Indian journal of nephrology, 2017-01, Vol.27 (1), p.66-68 |
| issn | 0971-4065 1998-3662 |
| language | eng |
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| subjects | Care and treatment Case Report Case studies Complications and side effects Diagnosis Hypophosphatemia Risk factors Tumors |
| title | Tumor-induced hypophosphatemia |
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