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.
Artículo
en Inglés
| 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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Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Síndromes Paraneoplásicos
/
Glándula Parótida
/
Vitamina D
/
Neoplasias de la Parótida
/
Hipofosfatemia
/
Adenoma Pleomórfico
/
Tejido Conectivo
/
Extremidad Inferior
/
Hipofosfatemia Familiar
/
Neoplasias de Tejido Conjuntivo
Tipo de estudio:
Estudio pronóstico
Límite:
Femenino
/
Humanos
Idioma:
Inglés
Revista:
Journal of the ASEAN Federation of Endocrine Societies
Año:
2016
Tipo del documento:
Artículo
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