Chen Qian, Cui Haocheng, Zheng Kai, Xu Ming, Yu Xiuchun
Department of Orthopedics, The 960th Hospital of the People's Liberation Army, Jinan, Shandong, China.
Front Oncol. 2024 Jul 25;14:1399021. doi: 10.3389/fonc.2024.1399021. eCollection 2024.
Primary intraosseous malignant peripheral nerve sheath tumors (MPNSTs) are rare yet highly aggressive neoplasms originating from peripheral nerves. Typically manifesting as soft tissue masses accompanied by pain or functional impairment, these tumors pose significant challenges in management. Surgical intervention remains the cornerstone of treatment for patients with MPNST lacking distant metastasis, with generally modest success rates. In cases of recurrence and metastasis, the pursuit of effective systemic therapies has been a focus of clinical investigation. Herein, we present a case study involving an elderly female patient with refractory MPNST. In light of surgical limitations, a multimodal therapeutic approach combining chemotherapy, denosumab, and subsequent administration of anlotinib was pursued following collaborative consultation. This regimen yielded noteworthy clinical benefits, exemplifying a promising avenue in the management of challenging MPNST cases.
原发性骨内恶性周围神经鞘瘤(MPNST)是一种罕见但侵袭性很强的肿瘤,起源于周围神经。这些肿瘤通常表现为伴有疼痛或功能障碍的软组织肿块,在治疗上带来了重大挑战。对于没有远处转移的MPNST患者,手术干预仍然是治疗的基石,但成功率一般不高。在复发和转移的情况下,寻求有效的全身治疗一直是临床研究的重点。在此,我们报告一例老年女性难治性MPNST患者的病例研究。鉴于手术的局限性,在多学科会诊后,采用了化疗、地诺单抗和随后使用安罗替尼的多模式治疗方法。该方案产生了显著的临床效益,为具有挑战性的MPNST病例的管理提供了一条有前景的途径。