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CASE REPORT
Year : 2019  |  Volume : 67  |  Issue : 8  |  Page : 1371-1373

A rare masquerade of chalazion: Adenoid cystic carcinoma


1 Oculoplasty and Ocular Oncology Services, Centre for Sight Hospital, New Delhi, India
2 Ocular Pathology Services, Centre for Sight Hospital, Hyderabad, Telangana, India

Correspondence Address:
Dr. Vikas Menon
Centre for Sight, B5/24, Safdarjung Enclave, New Delhi - 110 029
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijo.IJO_2009_18

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Adenoid cystic carcinoma (ACC) is a rarely seen malignant epithelial tumor of the eyelids. We present a rare case of primary ACC arising from the tarsal plate of the lower lid that clinically resembled a chalazion. A 66-year-old female presented with a recurring nodule in her left lower lid. She gave history of surgery for chalazion removal from the same site twice earlier. An initial diagnosis of a recurrent chalazion was made, and incision and curettage was done. Light microscopy showed a solid tumor composed predominantly of sheet-like and nested pattern of basaloid to low-columnar cells with intervening fibrovascular septa and lacking an obvious cribriform or tubular architecture. The tumor cells were positive for pan-cytokeratin and CD117 and negative for adipophilin, HMB45, and BerEP4. A diagnosis of solid variant of ACC of the eyelid was made. Wide excision was performed and eyelid defect was reconstructed.


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