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pubmed-article:20800492pubmed:abstractTextA sellar aspergillus abscess is a rare fungal infection of the central nervous system (CNS). A retrospective analysis of three patients with sellar aspergillus abscess was conducted from 2006 to 2008. Data were retrieved from patient records at our hospital. Clinical findings, pathological data and final outcomes were reviewed and analysed. All patients underwent transsphenoidal surgery with the operating microscope and histopathologic examination revealed aspergillosis in all cases. Postoperatively, all patients received medical treatment with voriconazole and caspofungin. During the 3-6-month follow-up period, the patients were symptom free with no recurrences. Therefore, sellar aspergillus abscess should be included in the differential diagnosis of a sellar mass. Early and correct diagnosis via surgery can improve the prognosis. A combination of surgical resection and antifungal therapy has a good outcome. The importance of early treatment for sellar aspergillus abscesses is emphasised.lld:pubmed
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pubmed-article:20800492pubmed:authorpubmed-author:OuJ CJClld:pubmed
pubmed-article:20800492pubmed:authorpubmed-author:DaumT ETElld:pubmed
pubmed-article:20800492pubmed:authorpubmed-author:BowenCaiClld:pubmed
pubmed-article:20800492pubmed:authorpubmed-author:LiGuopingGlld:pubmed
pubmed-article:20800492pubmed:authorpubmed-author:ChenHaifengHlld:pubmed
pubmed-article:20800492pubmed:authorpubmed-author:LiuWenkeWlld:pubmed
pubmed-article:20800492pubmed:copyrightInfoCopyright © 2010 Elsevier Ltd. All rights reserved.lld:pubmed
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pubmed-article:20800492pubmed:volume17lld:pubmed
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pubmed-article:20800492pubmed:year2010lld:pubmed
pubmed-article:20800492pubmed:articleTitleSuccessful treatment of sellar aspergillus abscess.lld:pubmed
pubmed-article:20800492pubmed:affiliationDepartment of Neurosurgery, West China Hospital, Sichuan University, Wuhou District, Chengdu 610041, China.lld:pubmed
pubmed-article:20800492pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20800492pubmed:publicationTypeCase Reportslld:pubmed