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首页> 外文期刊>Scottish medical journal >Pelvic inflammatory myofibroblastic tumour mimicking scrotal mass: an extremely rare case
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Pelvic inflammatory myofibroblastic tumour mimicking scrotal mass: an extremely rare case

机译:阴囊炎性盆腔炎性肌纤维母细胞瘤

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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.
机译:炎性肌纤维母细胞瘤(IMT)是一种罕见的良性间质肿瘤。但是,IMT可能来自多种组织,在老年人中非常罕见。 IMT可以模仿其起源。尽管IMT已被定义为不确定的行为,但仍可通过手术治疗。我们介绍了一个65岁的老人,其肿块被诊断为IMT,从阴囊延伸到骨盆。肿块与周围的任何解剖结构无关。据我们所知,这是文献中首例在老年人中诊断出骨盆IMT并经长期随访成功手术治疗的病例。 IMT的病因仍然未知,需要更多的研究来确定IMT的确切连续性。

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