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Updated: May 5, 2026

Surgical Treatment of an Endolymphatic Sac Tumor
Published on: May 26, 2023
Lacrimal sac squamous cell carcinoma: diagnostic challenges, surgical management and clinical outcomes
Paula Niinimäki1, Caj Haglund2,3, Hagström Jaana3,4
1Department of Ophthalmology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Purpose:
To evaluate the incidence, clinical features, diagnostic challenges, patient and healthcare-related delays, management, and outcomes of lacrimal sac squamous cell carcinoma (lsSCC) at a tertiary care centre.
Methods:
We identified patients from the Finnish Cancer Registry and the Helsinki University Hospital (HUS, Helsinki, Finland) databases over a 16-year period 2007-2022 and analysed clinical features, histopathology, human papillomavirus (HPV) positivity by immunohistochemical staining for p16INK4A (p16) and mRNA detection by in situ hybridization for high-risk HPV (HR-HPV), and treatment.
Results:
The median age at diagnosis for the 13 patients was 67 years (range, 40-97). Median time to histopathologic diagnosis of lsSCC was 6 months (range, 0-36). The most common reason for delay was treatment based on an incorrect diagnosis of dacryocystitis. Eye-sparing surgery was performed in eight (62%) and exenteration in five (38%) patients. Differentiation was classified as grade 2 in 38% and grade 3 in 62% of tumours. Eight of 12 analysed tumours (67%) were HPV positive. The reconstruction method involved a microvascular flap in 54% and a local pedicular skin or fascia flap in 46% of patients. Ten patients received postoperative external beam radiotherapy, and one patient received chemotherapy. The median follow-up time was 5 years (range, 0-17). The patient with regional micrometastasis developed systemic metastatic disease at 11 months and died of metastatic lsSCC 22 months after surgery.
Conclusion:
Two-thirds of the patients had an HR-HPV-positive tumour. Diagnosis of lsSCC is often delayed. Despite high tumour grade, recurrences and metastasis of lsSCC were rare in this cohort.
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