腱鞘巨细胞瘤和色素绒毛结节性滑膜炎。

IF 2.6 2区 医学 Q1 ORTHOPEDICS
Alysia K Kemp, Brian Brigman, Geoffrey Siegel, Charles A Popkin, Wakenda K Tyler
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引用次数: 0

摘要

腱鞘巨细胞瘤(tgct)是一种良性肿瘤,可发生在关节内和关节外。受累的类型也不同,从结节性,典型的小体积疾病到广泛和弥漫性滑膜浸润。手术切除仍然是大多数患者的治疗选择,切除技术包括关节镜、开放或联合入路。然而,TGCT可能具有局部侵袭性,即使在适当的手术切除后也表现出高复发率。对导致这些增殖性疾病的复杂遗传和环境因素的进一步了解使治疗方案现代化。发现肿瘤细胞集落刺激因子1的表达和炎症级联的传播的独特作用,导致使用辅助药物来改善预后。深入了解TGCT患者的病因、临床表现、诊断、检查、既往治疗和新的治疗方案对于骨科医生理解和有效地与多学科治疗团队合作至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tenosynovial Giant Cell Tumor and Pigmented Villonodular Synovitis.

Tenosynovial giant cell tumors (TGCTs) are a spectrum of benign growths that can occur in both intra-articular and extra-articular locations. The pattern of involvement also varies from nodular, typically small-volume disease to extensive and diffuse synovial infiltration. Surgical resection remains the treatment of choice for most patients and resection techniques include arthroscopic, open, or a combined approach. However, TGCT can be locally aggressive and exhibit high recurrence rates even after adequate surgical removal. Improved understanding of the complex genetic and environmental factors that lead to these proliferative disorders have modernized treatment options. Discovery of the unique role that tumor cell expression of the colony-stimulating-factor1 and propagation of the inflammatory cascade has led to the use of adjuvant medications to improve outcomes. In-depth knowledge of the etiology, clinical presentation, diagnosis, workup, historical treatments, and new treatment options for patients with TGCT are crucial for orthopaedic surgeons to understand and work effectively with a multidisciplinary treatment team.

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来源期刊
CiteScore
6.10
自引率
6.20%
发文量
529
审稿时长
4-8 weeks
期刊介绍: The Journal of the American Academy of Orthopaedic Surgeons was established in the fall of 1993 by the Academy in response to its membership’s demand for a clinical review journal. Two issues were published the first year, followed by six issues yearly from 1994 through 2004. In September 2005, JAAOS began publishing monthly issues. Each issue includes richly illustrated peer-reviewed articles focused on clinical diagnosis and management. Special features in each issue provide commentary on developments in pharmacotherapeutics, materials and techniques, and computer applications.
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