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
em En
| WPRIM
| ID: wpr-632791
Biblioteca responsável:
WPRO
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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Índice:
WPRIM
Assunto principal:
Síndromes Paraneoplásicas
/
Glândula Parótida
/
Vitamina D
/
Neoplasias Parotídeas
/
Hipofosfatemia
/
Adenoma Pleomorfo
/
Tecido Conjuntivo
/
Extremidade Inferior
/
Hipofosfatemia Familiar
/
Neoplasias de Tecido Conjuntivo
Tipo de estudo:
Prognostic_studies
Limite:
Female
/
Humans
Idioma:
En
Revista:
Journal of the ASEAN Federation of Endocrine Societies
Ano de publicação:
2016
Tipo de documento:
Article