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Tumour induced osteomalacia.
Author(s):
1. Muhammad Qamar Masood: Section of Endocrinology, The Aga Khan University Hospital, Karachi, Pakistan
2. Nanik Ram: Section of Endocrinology, The Aga Khan University Hospital, Karachi, Pakistan
3. Syed Ahsan Ali: Section of Internal Medicine, Department of Medicine, The Aga Khan University Hospital, Karachi, Pakistan
Abstract:
Tumour-induced osteomalacia (TIO) is a rare paraneoplastic syndrome usually presenting with bone pain, fracture of bones and muscle weakness. It is caused by high serum levels of fibroblast growth factor 23 (FGF- 23), which is a hormone-regulating phosphate, and vitamin D. FGF-23 is secreted by several tumours, especially benign mesenchymal tumours which are very small and difficult to locate. There is a significant delay from onset of symptoms to the diagnosis of this entity due to occult nature of this disease. We present a case of young male who presented with long history of progressively worsening muscular pain and weakness, rendering the patient confined to bed. Our aim of presenting this patient as a case report is to make physicians realise that any patient with unexplained muscular weakness and pain must undergo workup for TIO, including serum phosphate measurement, as this is a rare but potentially curable disease.
Page(s): 220-222
DOI: DOI not available
Published: Journal: Journal of Pakistan Medical Association, Volume: 65, Issue: 2, Year: 2015
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