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  • ArticleYalnız künye2015
    Pelvic inflammatory myofibroblastic tumour mimicking scrotal mass: an extremely rare case

    Aykan, Serdar; Akin, Yigit; Basara, Isil; Ates, Mutlu; Tuken, Murat; Uyar, Meral; Nuhoglu, Baris; Semercioz, Atilla

    Inflammatory myofibroblastic tumour (IMT) is a rare benign mesenchymal tumour. However, IMT may arise from a wide variety of tissues and is very rare in the elderly. IMT may mimic the mass in which it originates. Although IMT has been defined as uncertain behaviour, it is treated surgically. We present a-65-year old man whose mass was diagnosed as IMT extending from scrotum to pelvis. The mass was independent of any surrounding anatomic structures. According to our best knowledge this is the first case in the literature that pelvic IMT was diagnosed in an elderly man and successfully treated surgically with a long term follow-up period. Aetiology of IMT is still unknown, and more studies are needed for exact continuum of IMT.

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creativeworkseries.issn0036-9330
creativeworkseries.issn2045-6441
dc.date.accessioned2026-10-20T15:41:57.651160017Z
dc.date.available2026-10-20T15:41:57.651160017Z
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/24806
dc.publisherSAGE Publications Ltd
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleScottish Medical Journal
dspace.entity.typeJournal