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Indian J Pathol Microbiol ; 2007 Jul; 50(3): 565-7
Artículo en Inglés | IMSEAR | ID: sea-72815

RESUMEN

Adamantinoma of the long bones are uncommon, slow growing tumors with a predilection for the tibia. A special rare variant known as the osteofibrous dysplasia-like adamantinoma or differentiated adamantinoma is thought to be a precursor of the classic adamantinoma. We report a case in a 24 year old female who presented with pain and lytic lesion of the left tibia. Microscopy showed a tumor composed predominantly of osteofibrous dysplasia-like areas with focal cytokeratin positive epithelial islands. This case is highlighted because of its rarity, its association with good prognosis and possible misdiagnosis as osteofibrous dysplasia.


Asunto(s)
Adamantinoma/diagnóstico , Adulto , Neoplasias Óseas/diagnóstico , Femenino , Displasia Fibrosa Ósea/patología , Humanos , Tibia/patología
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