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DC Field | Value | Language |
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dc.contributor.author | Mombaerts I. | |
dc.contributor.author | Cameron J.D. | |
dc.contributor.author | Chanlalit W. | |
dc.contributor.author | Garrity J.A. | |
dc.date.accessioned | 2021-04-05T03:34:42Z | - |
dc.date.available | 2021-04-05T03:34:42Z | - |
dc.date.issued | 2014 | |
dc.identifier.issn | 1616420 | |
dc.identifier.other | 2-s2.0-84895069037 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14410 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84895069037&doi=10.1016%2fj.ophtha.2013.09.010&partnerID=40&md5=e7b2855f1d367ae7501bb7955d6016e1 | |
dc.description.abstract | Purpose Idiopathic inflammatory tumor of the lacrimal gland, also called idiopathic dacryoadenitis, generally is treated with high-dose, long-term systemic corticosteroids, despite their limited success, high recurrence rate, and incidence of drug-induced side effects. This study describes the outcome of patients with idiopathic dacryoadenitis who were managed with surgical debulking. Design Retrospective case series from 2 tertiary referral centers. Participants Forty-six patients (46 lacrimal glands). Methods Review of the clinical records, radiologic scans, and histopathologic specimens, with additional immunoglobulin G4 immunostaining. Main Outcome Measures Clinical signs and symptoms at 2 months after the surgery and off medications. Results Before referral, 41% (19 of 46) of the patients had received systemic high-dose corticosteroids, after which they all showed recurrence, of whom 26% (5 of 19) became dependent on corticosteroids. At referral, all patients underwent debulking surgery of the inflammatory lacrimal gland mass for diagnostic and therapeutic reasons. Additionally, intralesional or systemic low-dose corticosteroids were given during the operation or the first postoperative days in 54% (25 of 46) of the patients. At 2 months after the debulking surgery, a full clinical recovery was seen in 80% (37 of 46) of the patients. A recurrence occurred in 8% (3 of 37) of the patients 4 months and 2.2 and 4.6 years later. Surgical failure (20%; 9 of 46) was correlated with prior corticosteroid treatment (P = 0.002, Fisher exact test), but not with sclerosing inflammation present in 28% (13 of 46). The median follow-up time was 7.2 years (range, 0.7-18 years). Conclusions Debulking biopsy procedures for idiopathic dacryoadenitis, in addition to being diagnostic, may be therapeutic. © 2014 by the American Academy of Ophthalmology Published by Elsevier Inc. | |
dc.subject | corticosteroid | |
dc.subject | dexamethasone | |
dc.subject | immunoglobulin G4 | |
dc.subject | methotrexate | |
dc.subject | methylprednisolone | |
dc.subject | rituximab | |
dc.subject | triamcinolone | |
dc.subject | adolescent | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | Article | |
dc.subject | clinical article | |
dc.subject | clinical feature | |
dc.subject | corticosteroid therapy | |
dc.subject | cytoreductive surgery | |
dc.subject | dacryocystitis | |
dc.subject | drug megadose | |
dc.subject | female | |
dc.subject | histopathology | |
dc.subject | human | |
dc.subject | human tissue | |
dc.subject | idiopathic disease | |
dc.subject | immunohistochemistry | |
dc.subject | low drug dose | |
dc.subject | male | |
dc.subject | multicenter study (topic) | |
dc.subject | nuclear magnetic resonance imaging | |
dc.subject | treatment outcome | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Child | |
dc.subject | Dacryocystitis | |
dc.subject | Female | |
dc.subject | Follow-Up Studies | |
dc.subject | Humans | |
dc.subject | Lacrimal Apparatus | |
dc.subject | Magnetic Resonance Imaging | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Ophthalmologic Surgical Procedures | |
dc.subject | Retrospective Studies | |
dc.subject | Tomography, X-Ray Computed | |
dc.subject | Treatment Outcome | |
dc.subject | Young Adult | |
dc.title | Surgical debulking for idiopathic dacryoadenitis: A diagnosis and a cure | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Ophthalmology. Vol 121, No.2 (2014), p.603-609 | |
dc.identifier.doi | 10.1016/j.ophtha.2013.09.010 | |
Appears in Collections: | Scopus 1983-2021 |
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