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Scrotal Peripheral Primitive Neuroectodermal Tumor

机译:阴囊周围原始神经外胚层肿瘤

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摘要

The peripheral primitive neuroectodermal tumor (pPNET) is a rare malignant tumor originating from neuroectoderm that usually occurs in children or adolescent and is frequently located in the extremities, chest cavity, pelvic cavity and chest wall. We present a rare case of an 84-year-old man with a history of pPNET in the scrotal sac, to our knowledge not previously published in the literature. The presence of a large irreducible mass in the inguinal sac forced to exclude a tumor. Ultrasound and MRI are very useful modalities to assess the location of the mass, its dependency from any organ and the tumoral internal structure. Molecular imaging with the detection of EWS-FLI1 fusion transcripts is useful for the diagnosis and differential diagnosis of Ewing sarcoma/pPNETs.
机译:周围原始神经外胚层肿瘤(pPNET)是一种罕见的恶性肿瘤,起源于神经外胚层,通常发生于儿童或青少年中,通常位于四肢,胸腔,骨盆腔和胸壁。据我们所知,我们目前没有文献报道过一个罕见的病例,该病例是一个在阴囊中有pPNET病史的84岁男子。腹股沟囊中大量不可减少的肿块被迫排除肿瘤。超声和核磁共振成像是评估肿块位置,其对任何器官的依赖性以及肿瘤内部结构的非常有用的方法。检测EWS-FLI1融合转录本的分子成像可用于尤文肉瘤/ pPNETs的诊断和鉴别诊断。

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