马赛克局限性神经纤维瘤病复发性MPNST:一种罕见的情况

B. Abraham, Y. Marickar
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引用次数: 0

摘要

马赛克局部神经纤维瘤病是一种罕见的1型神经纤维瘤病(NF1)亚型,直到最近才被诊断出来。恶性周围神经鞘瘤(MPNST)在这种情况下的发生极为罕见,迄今文献报道仅5例。方法:通过检索PubMed和谷歌scholar获得的已发表病例报告进行叙述性综述。结果/讨论:复发模式及预后与常规MPNST不同。这些病例的组织学分级不一,但单独手术治疗可改善生存结果。尽管局部复发很常见,但这些病例均未出现远处转移。这与传统的MPNST形成对比,后者即使采用多种治疗方法也表现出较差的生存率和频繁的转移。由于其罕见性,尚未制定具体的治疗指南。结论:尽管组织形态学仍然是MPNST诊断的主要依据,但对这些病例进行进一步的细胞遗传学和分子分析对于发明新的靶向药物至关重要。在这篇综述中,我们讨论了这种罕见实体的临床结果,并强调了了解分子事件对未来靶向治疗的重要性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent MPNST in Mosaic Localized Neurofibromatosis: A Rare Scenario – Review
Introduction: Mosaic localized neurofibromatosis is a rare subtype of Neurofibromatosis type 1 (NF1) which is largely underdiagnosed till recently. The occurrence of Malignant Peripheral Nerve Sheath Tumor (MPNST) in such a setting is extremely rare with only 5 cases reported in literature till date. Method: Narrative review based on published case reports, obtained by searching on PubMed and Google scholar. Results/ Discussion: The pattern of recurrence and prognosis are different from conventional MPNST. The cases are of variable histologic grade, but showed improved survival outcome with surgical treatment alone. Even though local recurrence is common, none of these cases showed distant metastasis. This is in contrast with conventional MPNST which shows poor survival and frequent metastasis even with multimodality treatment. Specific treatment guidelines are yet to be established because of its rarity. Conclusions: Even though histomorphology remains the mainstay of diagnosis of MPNST, further cytogenetic and molecular analysis of these cases are crucial in the invention of new targeted drugs. In this review, we discuss the clinical outcome of this rare entity and highlight the importance of understanding the molecular events for future targeted
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