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Journal of the Korean Ophthalmological Society ; : 1257-1262, 1996.
Artigo em Coreano | WPRIM | ID: wpr-23830

RESUMO

Primary lymphocytic tumor of the orbit is known as a relatively uncommon condition and difficult to diagnose in their types exactly even with microscopic examination. The authors experienced a reactive lymphoid hyperplasia patient, 42 years old male, which was progressed to atypical lymphoid hyperplasia during 4 years, confirmed by immunoperoxidase staining. In this case, steroid therapy was of no use and it shows resistance to combined chernotherapy.


Assuntos
Adulto , Humanos , Masculino , Hiperplasia , Órbita , Pseudolinfoma
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