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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/2226


    Title: Carcinoid tumor of the middle ear: a case report
    Authors: Chan, KC;Wu, CM;Huang, SF
    Contributors: Division of Molecular and Genomic Medicine
    Abstract: Middle ear (ME) carcinoid tumor is exceedingly rare. We present a case of ME carcinoid tumor in a 29-year-old woman whose chief complaints were right otalgia, aural fullness, hearing loss, and facial palsy of 5 days duration. A reddish bulging mass behind the right eardrum and right facial palsy staged as grade IV on the House-Brackmann scale were noted. The high-resolution computed tomography of the temporal bone showed a soft-tissue density mass in the right middle ear and antrum without bony invasion. Although the initial diagnosis was ME adenoma made by the intraoperative frozen section report, the tumor was resected completely by a modified conservative ossicles-preservation method. The patient's initial symptoms of otalgia, aural fullness, and hearing loss immediately improved after surgery, and facial palsy diminished in the following months. No recurrence was noted after 12 months of follow-up. (C) 2005 Elsevier Inc. All rights reserved.
    Keywords: Otorhinolaryngology
    Date: 2005-01
    Relation: American Journal of Otolaryngology. 2005 Jan-Feb;26(1):57-59.
    Link to: http://dx.doi.org/10.1016/j.amjoto.2004.06.011
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0196-0709&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000226557300012
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=11144340300
    Appears in Collections:[黃秀芬] 期刊論文

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