*Corresponding author:
Kelmend Spahiu, Department of Ophthalmology, Prishtina, Kosova, Postal Code: 10000, Republic of KosovoReceived: March 25, 2018; Published: April 11, 2018
DOI: 10.26717/BJSTR.2018.03.000952
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Back ground: 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.
Keywords: Lacrimal Gland; Adenocarcinoma NOS;Neoplasia; Exenteration
Abstract Introduction| Case Report| Discussion| Conclusion| References|