Sugiura Yoshiki, Nagaishi Masaya, Takano Issei, Tanaka Yoshihiro, Suzuki Kensuke, Yokoo Hideaki, Hyodo Akio
Clin Neuropathol. 2015 Jan-Feb;34(1):13-8. doi: 10.5414/NP300785.
Chondromas are rare benign tumors that commonly originate from the base of the skull, while those arising from the dura mater are less common. Although the molecular mechanism underlying its pathogenesis remains largely unknown, 12q13-15 rearrangements followed by the activation of HMGA2, which is associated with cell proliferation, have been reported in soft tissue chondromas. A recent comprehensive analysis of mesenchymal tumors identified an IDH1/2 mutation in cartilaginous tumors. However, these alterations have not yet been examined in dural chondromas. We here described clinical and pathological features in a new case of convexity dural chondroma with the wildtype IDH1/2 and expression of HMGA2 and reviewed the relevant literature.
软骨瘤是罕见的良性肿瘤,通常起源于颅底,而起源于硬脑膜的软骨瘤则较少见。尽管其发病机制的分子机制在很大程度上仍不清楚,但在软组织软骨瘤中已报道有12q13 - 15重排,随后HMGA2激活,这与细胞增殖有关。最近一项对间叶性肿瘤的综合分析在软骨肿瘤中发现了IDH1/2突变。然而,这些改变尚未在硬脑膜软骨瘤中进行研究。我们在此描述了一例具有野生型IDH1/2且HMGA2表达的凸面硬脑膜软骨瘤新病例的临床和病理特征,并复习了相关文献。