一个不寻常的实体:鼻腔软组织巨细胞瘤

Nur Khairul Bariyyah Mohd Hatta, N. Saifudin
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引用次数: 0

摘要

软组织巨细胞瘤(GCT-ST)是一种罕见的软组织肿瘤,第一例报道于20世纪70年代。累及头颈部,尤其是鼻腔是极为罕见的。GCT-ST被认为是骨对应物,具有显著的组织学和免疫组织化学相似性。尽管如此,骨骼的GCT- st和GCT在基因上是不同的。显微镜下,GCT-ST显示大量破骨细胞型多核巨细胞,背景为单核间质细胞。它们是局部侵袭性的,有可能复发。区分GCT-ST和巨细胞修复性肉芽肿(GCRG)很重要,因为它们具有相似的临床和形态学特征,但它们有不同的治疗方式。我们报告一例GCT-ST发生在鼻腔,一个不寻常的表现部位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Unusual Entity: Giant Cell Tumour of Soft Tissue in the Nasal Cavity
Giant cell tumour of soft tissue (GCT-ST) are rare soft tissue tumours, with the first case reported in the 1970s. Involvement of the head and neck region, particularly in the nasal cavity is extremely uncommon. GCT-ST are considered the bone counterpart given the striking histological and immunohistochemical resemblance. Despite that, GCT-ST and GCT of bones are genetically distinct. Microscopically, GCT-ST exhibit numerous osteoclast-type multinucleated giant cells within a background of mononuclear stromal cells. They are locally aggressive and can potentially recur. It is important to distinguish GCT-ST from giant cell reparative granuloma (GCRG) as they both share similar clinical and morphological characteristics, however, they have different treatment modalities. We report a case of GCT-ST occurring in the nasal cavity, an unusual site of presentation.
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