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首页> 外文期刊>Targeted oncology >Partial response of a rare malignant metastatic diffuse tenosynovial giant cell tumor with benign histologic features, treated with SCH 717-454, an insulin growth factor receptor inhibitor, in combination with everolimus, an MTOR inhibitor
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Partial response of a rare malignant metastatic diffuse tenosynovial giant cell tumor with benign histologic features, treated with SCH 717-454, an insulin growth factor receptor inhibitor, in combination with everolimus, an MTOR inhibitor

机译:用胰岛素生长因子受体抑制剂SCH 717-454和MTOR抑制剂依维莫司联合治疗罕见的具有良性组织学特征的罕见恶性转移性腱鞘内巨细胞瘤

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摘要

Tenosynovial giant cell tumor (TGCT) is a neoplastic proliferation arising in tendon sheath, bursa, and/or synovium.Decades ago, it was thought to be an inflammatory process, owing to the presence of large numbers of macrophages within the tumor. However, TGCT is now considered a neoplastic process composed of compact foci of polyhedral cells with varying numbers of multinucleated giant, lipid, and hemosiderin-laden cells. These tumors can be subdivided based on the degree of synovial involvement into localized (circumscribed) or diffuse forms. Localized TGCT tends to occur in the finger and is nodular. Though it may recur, it is generally amenable to local resection. On the other hand, diffuse type TGCT more frequently affects larger joints, especially the knee and wrist. This diffuse type can be intra-articular (also called pigmented villonodular tenosynovitis) or extra-articular, and is notoriously difficult to control with local resection, tending to recur frequently.
机译:腱鞘巨细胞瘤(TGCT)是一种在肌腱鞘,法氏囊和/或滑膜中发生的赘生物增生。数十年前,由于肿瘤内存在大量巨噬细胞,因此被认为是炎症过程。然而,TGCT现在被认为是由多面体细胞的紧密灶和不同数量的多核巨细胞,脂质和含铁血黄素的细胞组成的肿瘤形成过程。这些肿瘤可根据滑膜受累程度分为局部(外接)或弥散性。 TGTG局部发生在手指上,呈结节状。尽管它可能复发,但通常适合局部切除。另一方面,弥漫型TGCT更常影响较大的关节,尤其是膝盖和手腕。这种弥漫性类型可以是关节内(也称为色素沉着绒毛腱鞘性腱鞘炎)或关节外的,众所周知,局部切除难以控制,往往会复发。

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