Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/27249
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dc.contributor.authorUeathaweephol S.
dc.contributor.authorWongwattana P.
dc.contributor.authorChanlalit W.
dc.contributor.authorTrongwongsa T.
dc.contributor.authorSutthinont S.
dc.date.accessioned2022-12-14T03:17:02Z-
dc.date.available2022-12-14T03:17:02Z-
dc.date.issued2022
dc.identifier.issn22871152
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85125940464&doi=10.7181%2facfs.2022.00612&partnerID=40&md5=f4d308edc65d999c3e77e9d046cc9eed
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/27249-
dc.description.abstractPrimary lymphoma originating from the lacrimal drainage system is a rare disease. Such lymphomas are mostly B-cell in origin and present nonspecific symptoms. The treatment of malignant lymphoma of the lacrimal drainage system is slightly different. We present the case of a 71-year-old woman with a painless mass below the medial canthus. Computed tomography (CT) scan of the orbit revealed a mass invading the right lacrimal sac. An incision biopsy was obtained, and the pathologic findings suggested a diagnosis of primary diffuse large B-cell lymphoma of the lacrimal sac. The patient was treated with chemotherapy and intrathecal methotrexate. After completing eight cycles of chemotherapy, the patient was followed up by a CT scan, which revealed nearly total resolution of an ill-defined enhancing mass. At the time of this case report writing, the patient is in complete remission at six months with no other complications. © 2022 Korean Cleft Palate-Craniofacial Association.
dc.languageen
dc.publisherKorean Cleft Palate-Craniofacial Association
dc.subjectCase reports
dc.subjectDiffuse large B-cell lymphoma
dc.subjectLacrimal sac
dc.subjectLymphoma
dc.subjectNasolacrimal sac
dc.titleLacrimal sac lymphoma: a case report
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationProceedings - 2022 IEEE 11th International Conference on Communication Systems and Network Technologies, CSNT 2022. Vol , No. (2022), p.612-615
dc.identifier.doi10.7181/acfs.2022.00612
Appears in Collections:Scopus 2022

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