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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