恶性周围神经鞘肿瘤表现为神经纤维瘤病患者股骨病理性骨折

R. Khan, S. Rehman, V. Maheshwari, K. Alam
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引用次数: 0

摘要

恶性外周神经鞘肿瘤(MPNSTs)是一种罕见的软组织肉瘤,由外周神经或与神经鞘相关的细胞,如雪旺细胞、神经周围细胞或成纤维细胞引起。MPNST占所有软组织肉瘤的5%-10%。神经纤维瘤病-1(NF-1)中的神经纤维瘤可能在2%-5%的患者中发生恶性转化。我们报告了一例非常罕见的NF-1患者,其表现为病理性股骨粗隆间骨折和肝转移。左髋关节X线片显示溶解性病变,经组织病理学检查为MPNST。S-100阳性,证实其神经起源。后来切除的肘部病变也表现出类似的S-100阳性特征。腹部超声检查显示肝脏有靶向病变。肝细针穿刺细胞学检查显示散在的恶性梭形细胞。最终诊断为转移性MPNST。尽管神经纤维瘤的恶性转化发生时极为罕见,但75%的患者与NF-1相关。该病例强调了恶性转化的NF患者股骨骨折的可能性,正如报告所述。该病例在其表现和转移部位的罕见性方面是独特的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malignant peripheral nerve sheath tumor presenting as pathological fracture of femur in neurofibromatosis patient
Malignant peripheral nerve sheath tumors (MPNSTs) are rare soft tissue sarcomas that arise from a peripheral nerve or cells associated with the nerve sheath, such as Schwann cells, perineural cells, or fibroblasts. MPNSTs account for 5%–10% of all soft tissue sarcomas. Neurofibromas in Neurofibromatosis-1 (NF-1) may undergo malignant transformation in 2%–5% of patients. We are reporting a very rare case in NF-1 patient who, presented with pathological intertrochanteric fracture of femur and liver metastasis. X-ray from left hip joint shows lytic lesion which on histopathology turned out to be MPNST. S-100 was positive confirming its neural origin. Elbow lesion which was excised later, also showed similar features with S-100 positivity. Ultrasonography abdomen showed target lesions in liver. Fine-needle aspiration cytology from liver showed scattered malignant spindle cells. A final diagnosis of metastatic MPNST was made. Although malignant transformation in neurofibromas is extremely rare when it occurs, it is associated with NF-1 in 75% of patients. This case highlights the possibility of fracture femur as the presenting complains, in patients of NF with malignant transformation. The case is unique with regard to its presentation and rarity of metastatic sites.
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