腰肌孤立性神经纤维瘤:一个不寻常的位置

C. Chaturvedi, H. Chaturvedi
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引用次数: 0

摘要

神经纤维瘤是一种良性周围神经鞘肿瘤,通常出现在头部和躯干的浅表组织。神经纤维瘤位于腹膜后极为罕见,仅占所有腹膜后肿瘤的1%。它可能是孤立的,也可能与遗传疾病、冯·雷克林豪森病或1型神经纤维瘤病有关。磁共振成像(MRI)是腹膜后肿瘤成像的金标准方式,因为它在评估病变的位置、范围和组成方面提供了更好的定义和特异性。在这里,我们报告一例30岁的男性腹膜后孤立性腰肌神经纤维瘤,但与von Recklinghausen病无关。MRI显示右侧腰肌腹膜后可见明确的分叶状病变。手术完全切除肿瘤,并通过组织学和免疫组织化学检查诊断为神经纤维瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Solitary neurofibroma of the psoas muscle: An unusual location
Neurofibroma is a benign peripheral nerve sheath tumour usually present on superficial tissues of the head and trunk. Retroperitoneal location is extremely rare for neurofibroma and comprises only 1% of all retroperitoneal tumours. It can be solitary or associated with the genetic disorder, von Recklinghausen's disease or neurofibromatosis type-1. Magnetic resonance imaging (MRI) is the gold standard modality for imaging retroperitoneal tumours because it provides a better definition and specificity in the evaluation of the location, extension, and composition of the lesion. Here, we report the case of a 30-year-old man affected by retroperitoneal solitary neurofibroma of the psoas muscle, but not associated with von Recklinghausen's disease. MRI showed a well-defined lobulated retroperitoneal lesion noted within the right psoas muscle. Complete surgical excision of the tumour was performed, and the diagnosis of neurofibroma was made through histological and immunohistochemical examination.
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