{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T20:32:00Z","timestamp":1787776320844,"version":"build-2784847793"},"reference-count":17,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Mantle cell lymphoma (MCL) of the lacrimal sac is an exceptionally rare tumor with only four such cases reported in literature, to the best of authors\u2019 knowledge. The tumor is known to have extensive systemic and bone marrow involvement with poor prognosis and overall survival. The present case describes a 64-year-old male with primary MCL of the lacrimal drainage system, its diagnosis, and treatment options.<\/jats:p>","DOI":"10.4103\/sjopt.sjopt_66_25","type":"journal-article","created":{"date-parts":[[2025,5,24]],"date-time":"2025-05-24T03:04:16Z","timestamp":1748055856000},"page":"185-187","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Mantle cell lymphoma of the lacrimal drainage system: A rare case and review of literature"],"prefix":"10.4103","volume":"39","author":[{"given":"Nandini","family":"Bothra","sequence":"first","affiliation":[{"name":"Govindram Seksaria Institute of Dacryology, L.V Prasad Eye Institute, Hyderabad, Telengana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mohammad J.","family":"Ali","sequence":"additional","affiliation":[{"name":"Govindram Seksaria Institute of Dacryology, L.V Prasad Eye Institute, Hyderabad, Telengana, 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