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Case report of tumour-induced osteomalacia with parotid gland tumour as a focus / Journal of the ASEAN Federation of Endocrine Societies
Journal of the ASEAN Federation of Endocrine Societies ; : 171-177, 2016.
Article Dans Anglais | WPRIM | ID: wpr-632791
ABSTRACT
@#<p style="text-align justify;">Tumour-induced osteomalacia (TIO) is a rare paraneoplastic syndrome, which is characterized by overproduction of FGF23 as a phosphaturic agent leading to chronic phosphaturia and hypophosphatemia, associated with inappropriately normal or low levels of vitamin D. We describe a rare case of a 57-year-old Indian female who presented with bone pains, muscle pains and lower limb weakness. On examination she was found to have hypophosphatemia. Our work up led to the identification of a FGF23 secreting parotid tumour. The tumour responsible for symptoms was a pleomorphic adenoma of the parotid gland. Its complete resection resulted in normalisation of patient's symptoms. Laboratory parameters and microsopic examination further revealed a mesenchymal tumour of mixed connective tissue type.</p>
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Indice: WPRIM (Pacifique occidental) Sujet Principal: Syndromes paranéoplasiques / Glande parotide / Vitamine D / Tumeurs de la parotide / Hypophosphatémie / Adénome pléomorphe / Tissu conjonctif / Membre inférieur / Hypophosphatémie familiale / Tumeurs du tissu conjonctif Type d'étude: Étude pronostique Limites du sujet: Femelle / Humains langue: Anglais Texte intégral: Journal of the ASEAN Federation of Endocrine Societies Année: 2016 Type: Article

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Indice: WPRIM (Pacifique occidental) Sujet Principal: Syndromes paranéoplasiques / Glande parotide / Vitamine D / Tumeurs de la parotide / Hypophosphatémie / Adénome pléomorphe / Tissu conjonctif / Membre inférieur / Hypophosphatémie familiale / Tumeurs du tissu conjonctif Type d'étude: Étude pronostique Limites du sujet: Femelle / Humains langue: Anglais Texte intégral: Journal of the ASEAN Federation of Endocrine Societies Année: 2016 Type: Article