Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/19378
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dc.contributor.authorSomtaporn Ueathaweepholth_TH
dc.contributor.authorPanuwat Wongwattanath_TH
dc.contributor.authorWaruttaporn Chanlalitth_TH
dc.contributor.authorTherdkiat Trongwongsath_TH
dc.contributor.authorSirilak Sutthinontth_TH
dc.date.accessioned2022-03-28T06:12:39Z-
dc.date.available2022-03-28T06:12:39Z-
dc.date.issued2022-
dc.identifier.urihttps://e-acfs.org/upload/pdf/acfs-2022-00612.pdf-
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/19378-
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.th_TH
dc.language.isoenth_TH
dc.subjectCase reportsth_TH
dc.subjectDiffuse large B-cell lymphomath_TH
dc.subjectNasolacrimal sacth_TH
dc.subjectLacrimal sacth_TH
dc.subjectLymphomath_TH
dc.titleLacrimal sac lymphoma: a case reportth_TH
dc.typeArticleth_TH
dc.identifier.bibliograpycitationArch Craniofac Surg Vol.23 No.1, 43-47th_TH
dc.identifier.doihttps://doi.org/10.7181/acfs.2022.00612-
Appears in Collections:Med-Journal Articles

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