Adenocarcinoma of Lacrimal Gland Non Otherwise Specified - A Case Report

Abstract

Background: Lacrimal gland adenocarcinoma is very rare tumor and highly agrressive. Methods:A 86-year-old woman presented with a 5-month history of a painless mass in the right uppereyelid. The clinical presentation, workup, surgical approach, and pathological findings were reviewed.Results: Incisional biopsy was performed toconfirm diagnosis. After histopathologicalconfirmation,exenteration was undergone and follows up further to oncology department. Conclusion:Tumors of lacrimal gland are highly aggressive but fortunately are very rare. In invasive cases complete excision of tumor, or exenteration with adjuvant radiotherapy and chemotherapy is highly recommended.