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Article in Korean | WPRIM (Western Pacific) | ID: wpr-23830

ABSTRACT

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.


Subject(s)
Adult , Humans , Male , Hyperplasia , Orbit , Pseudolymphoma
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