MESENCHYMAL PHOSFATURIC TUMOR: A CASE REPORT OF SUCCESS
Introduction/Justification: Hypophosphatemia mesenchymal tumors (HMT) are rare, of uncertain origin, and may cause osteomalacia derived from paraneoplastic syndrome. The clinical manifestations are caused mainly by phosphatase secretion promoted by the tumor cells, leading to excessive kidney excret...
| الحاوية / القاعدة: | Hematology, Transfusion and Cell Therapy |
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| المؤلفون الرئيسيون: | , , , , , |
| التنسيق: | مقال |
| اللغة: | الإنجليزية |
| منشور في: |
Elsevier
2025-05-01
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| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.sciencedirect.com/science/article/pii/S2531137925000847 |