Lacrimal sac lymphoma: a case series and literature review
Autor: | Feng-Xi Meng, Han Yue, Yi-Qun Yuan, Rui Zhang, Yi-Fei Yuan, Ying-Wen Bi, Jiang Qian |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: | |
Zdroj: | International Journal of Ophthalmology, Vol 15, Iss 10, Pp 1586-1590 (2022) |
Druh dokumentu: | article |
ISSN: | 2222-3959 2227-4898 |
DOI: | 10.18240/ijo.2022.10.04 |
Popis: | AIM: To study the clinical and pathological characteristics of the lacrimal sac lymphoma, which is rare but it is the major type of non-epithelial malignant tumor in the lacrimal sac region. METHODS: Sixty-four cases of malignant lacrimal sac tumors in our hospital from 1986 to 2020 were retrospectively reviewed. Eight cases of lacrimal sac lymphoma were carefully reviewed. RESULTS: There were five mucosal-associated lymphoid tissue (MALT) lymphomas, one diffused large B-cell lymphoma, one NK/T cell lymphoma, and one mantle cell lymphoma. All eight patients represented symptoms of epiphora with swelling in the lacrimal sac for a certain period of time and showed no signs of systemic involvement at the first time of clinical visits. They had received either chemotherapy or radiotherapy after surgery. Long-term follow-up (from 11 to 220mo) showed that, except one patient with MALT lymphoma died for unknown reasons at 104mo after surgery, the other 7 patients were all alive with no signs of local recurrence, neither in other organs. CONCLUSION: Non-epithelial malignant tumors of the lacrimal sac are rare and lymphoma is the major subtype. |
Databáze: | Directory of Open Access Journals |
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