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酷似阴囊肿物的盆腔炎性肌纤维母细胞瘤:1例极其罕见的病例

Pelvic inflammatory myofibroblastic tumour mimicking scrotal mass: an extremely rare case.

作者信息

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

机构信息

M.D., Department of Urology, Bagcilar Research and Training Hospital, Turkey.

Assistant Professor of Urology, Department of Urology, School of Medicine, Harran University, Turkey.

出版信息

Scott Med J. 2015 Feb;60(1):e8-10. doi: 10.1177/0036933014563240. Epub 2014 Dec 2.

Abstract

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.

摘要

炎性肌纤维母细胞瘤(IMT)是一种罕见的良性间叶组织肿瘤。然而,IMT可起源于多种组织,在老年人中极为罕见。IMT可能会模仿其起源部位的肿块。尽管IMT的行为被定义为不确定,但仍采用手术治疗。我们报告一名65岁男性,其肿块被诊断为从阴囊延伸至骨盆的IMT。该肿块与周围任何解剖结构均无关联。据我们所知,这是文献中首例在老年男性中诊断出盆腔IMT并通过长期随访成功进行手术治疗的病例。IMT的病因仍不清楚,需要更多研究来明确IMT的确切发展过程。

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