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Journal of the Korean Radiological Society ; : 29-31, 1997.
Artículo en Coreano | WPRIM | ID: wpr-79829

RESUMEN

Langerhans cell histiocytosis(LCH) is a systemic disorder characterized by idiopathic proliferation of histiocytes in the reticuloendothelial system; CNS involvement outside the hypothalamus or pituitary gland is uncommon. We present a case of LCH involving the brainstem, cerebellum, and temporal lobes, and also showing hypothalamic involvement. The lesions were isointense or hypointense on T1WI and hyperintense on T2WI, and showed multifocal enhancing nodules on post-contrast CT and Gd-enhanced MRI.


Asunto(s)
Tronco Encefálico , Sistema Nervioso Central , Cerebelo , Histiocitos , Histiocitosis , Histiocitosis de Células de Langerhans , Hipotálamo , Imagen por Resonancia Magnética , Sistema Mononuclear Fagocítico , Hipófisis , Lóbulo Temporal
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