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Lacrimal sac lymphoproliferative lesion: case report
I Coloma-González1, L Ruíz-García1, A Ceriotto1
1Servicio de Párpados, Órbita y Vía Lagrimal, Asociación para evitar la Ceguera IAP, Hospital Dr. Luis Sánchez Bulnes, México DF, México.
Case Report:
The case is presented of a 51 year-old woman with a firm mass at the medial canthus of the right eye of five years onset. A low-grade lymphoproliferative lesion (reactive lymphoid hyperplasia) was diagnosed from an excisional biopsy
Discussion:
Lacrimal sac tumors are rare, with a peak incidence in the fifth decade of life. The initial clinical features are epiphora and medial canthus swelling. As it mimics nasolacrimal duct obstruction, up to 40% of these tumors are misdiagnosed until undergoing surgery.

