Sinonasal renal cell-like adenocarcinoma: Easily misdiagnosed sinonasal tumor.

CN Wu, IC Chuang, MJ Chuang, Wei-Chih Chen

    研究成果: 期刊稿件文章同行評審

    6 引文 斯高帕斯(Scopus)

    摘要

    Sinonasal renal cell-like adenocarcinoma is rare and exhibits unique pathological and clinical manifestations. Correct diagnosis and treatment of this newly described entity are challenging for both clinicians and pathologists. We report a female patient with sinonasal renal cell-like adenocarcinoma who initially presented with right intermittent epistaxis. A 26-year-old woman presented with a 1-year history of right intermittent epistaxis and hyposmia. Nasal endoscopy revealed a reddish tumor in the right nasal cavity. An MRI revealed a hyperintense tumor arising from the right olfactory cleft accompanied by prominent feeding vessels originating from the anterior ethmoid artery (AEA). We performed a bicoronal incision with ligation of the AEA followed by endoscopic resection of the skull base tumor. The patient is currently free of recurrence. This is the first study to review the clinical features of sinonasal renal cell-like adenocarcinoma. We recommend surgical resection as the mainstay of treatment.
    原文美式英語
    期刊Head & neck
    40
    發行號9
    DOIs
    出版狀態已出版 - 2018

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