Jeon Yoon-Kyung, Cheon Jung-Eun, Kim Seung-Ki, Wang Kyu-Chang, Cho Byung-Kyu, Park Sung-Hye
Department of Pathology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Mod Pathol. 2008 Nov;21(11):1345-56. doi: 10.1038/modpathol.2008.88. Epub 2008 Jul 11.
Pilomyxoid astrocytoma is a recently identified variant of pilocytic astrocytoma. We studied 11 circumscribed astrocytomas with focal (n=5) or diffuse (n=6) pilomyxoid features and compared them with 17 pilocytic astrocytomas from the hypothalamic/chiasmatic region in children. In one patient, a tumor that recurred after initial surgery had changed from pure-form pilomyxoid astrocytoma to the mixed form. The presence of a pilomyxoid area was associated with shorter survival. Next, we compared the comprehensive genome copy number changes in the pilomyxoid astrocytoma (n=4) with those in pilocytic astrocytoma (n=6) cases by array-based comparative genomic hybridization. The number of lost clones was larger in pilomyxoid astrocytoma than in pilocytic astrocytoma. Clones located in chromosome 8q24.3 were frequently gained in pilocytic astrocytoma (four of six) and in pilomyxoid astrocytoma (one of four). Clones located in 9p24.3 and 15q26.3 were lost in all of the pilomyxoid astrocytomas and in five of the pilocytic astrocytomas. Those in 8p23.3 showed a copy number loss in three of the pilomyxoid astrocytomas and four of the pilocytic astrocytomas. The frequency of copy number changes was significantly different between pilomyxoid astrocytoma and pilocytic astrocytoma in 47 (3.6%) clones, 20 of them having been located in 2p, 10 in 2q, and 11 in 3q. An unsupervised hierarchical clustering analysis classified the cases into three clusters: one pilomyxoid astrocytoma patient into one cluster, two pilomyxoid astrocytoma patients into another cluster, and six pilocytic astrocytoma patients and one pilomyxoid astrocytoma patient into the third cluster. In conclusion, the presence of mixed-form pilomyxoid astrocytoma, the acquisition of pilocytic astrocytoma features in a recurrent tumor in pure-form pilomyxoid astrocytoma, and the above results of the genome-wide gene copy number analysis suggest that pilomyxoid astrocytoma might be a pathologically and genetically related, aggressive variant of pilocytic astrocytoma with partially different genetic alterations.
毛黏液样星形细胞瘤是最近发现的毛细胞型星形细胞瘤的一种变体。我们研究了11例具有局灶性(n = 5)或弥漫性(n = 6)毛黏液样特征的局限性星形细胞瘤,并将其与17例儿童下丘脑/视交叉区域的毛细胞型星形细胞瘤进行比较。在1例患者中,初始手术后复发的肿瘤已从纯形式的毛黏液样星形细胞瘤转变为混合形式。毛黏液样区域的存在与较短的生存期相关。接下来,我们通过基于阵列的比较基因组杂交,比较了毛黏液样星形细胞瘤(n = 4)和毛细胞型星形细胞瘤(n = 6)病例的全基因组拷贝数变化。毛黏液样星形细胞瘤中丢失的克隆数比毛细胞型星形细胞瘤多。位于染色体8q24.3的克隆在毛细胞型星形细胞瘤(6例中的4例)和毛黏液样星形细胞瘤(4例中的1例)中经常获得。位于9p24.3和15q26.3的克隆在所有毛黏液样星形细胞瘤以及5例毛细胞型星形细胞瘤中丢失。位于8p23.3的克隆在3例毛黏液样星形细胞瘤和4例毛细胞型星形细胞瘤中显示拷贝数丢失。在47个(3.6%)克隆中,毛黏液样星形细胞瘤和毛细胞型星形细胞瘤的拷贝数变化频率存在显著差异,其中20个位于2p,10个位于2q,11个位于3q。无监督层次聚类分析将病例分为三个簇:1例毛黏液样星形细胞瘤患者分为一个簇,2例毛黏液样星形细胞瘤患者分为另一个簇,6例毛细胞型星形细胞瘤患者和1例毛黏液样星形细胞瘤患者分为第三个簇。总之,混合形式毛黏液样星形细胞瘤的存在、纯形式毛黏液样星形细胞瘤复发肿瘤中获得毛细胞型星形细胞瘤特征以及上述全基因组基因拷贝数分析结果表明,毛黏液样星形细胞瘤可能是毛细胞型星形细胞瘤在病理和遗传上相关的侵袭性变体,具有部分不同的基因改变。