Hiemcke-Jiwa L S, van Ewijk R, van Noesel M M, Tops B B J, Koppes S A, Lubeek S F K, Jonges G N, Witkamp A J, von Deimling A, Cleven A H G, Kester L A, Flucke U
Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Princess Maxima Center for Pediatric Oncology, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Virchows Arch. 2025 Aug 14. doi: 10.1007/s00428-025-04211-5.
GLI1/2 alterations drive mesenchymal tumors harboring rearrangements and amplifications. Affected patients show a broad age range and tumor distribution, and histology varies. We describe the clinicopathologic and molecular characteristics of eight cases (7 females, 1 male, age range 15-82 years). Tumors were located in the ovary (n = 3), endometrium (n = 1), retroperitoneum (n = 1), skin (n = 1), neck (n = 1), and hypopharynx (n = 1). The cases showed epithelioid (n = 2), spindle cell (n = 1), biphasic (n = 1), or round cell (n = 3) morphology. Two of the latter neoplasms had a prominent myxoid stroma. One tumor was polymorphic with brisk mitotic activity. Immunohistochemistry demonstrated variable positivity for S100, pankeratin AE1/3, EMA, CD56, synaptophysin and chromogranin. MDM2, CDK4, and STAT6 expressions were detected in cases with GLI1 amplification. In three neoplasms, a fusion gene was identified (GLI1::MALAT1, n = 2; PTBP1::GLI2, n = 1). Three cases harbored GLI1-amplification, with co-amplification of MDM2/CDK4 in two of them. GLI2 was amplified in one tumor. Another case had an inactivating PTCH1 mutation. By RNA expression and DNA methylation profiling, the cases formed a cluster. GLI-amplified tumors occurred in older patients (n = 3) who died within 3-27 months. GLI-fusion genes and the PTCH1 mutation were identified in neoplasms of younger patients (n = 3) remaining disease-free (25-31 months). In conclusion, our GLI1/2 altered mesenchymal tumors, clustered at RNA level and epigenetically, confirming that they form one entity, including neoplasms with PTCH1 mutations. Amplified tumors occurred in older patients and behaved more aggressively, in contrast to lesions with a fusion gene originating in younger patients and showing a favorable outcome.
GLI1/2改变驱动具有重排和扩增的间叶性肿瘤。受影响的患者年龄范围广,肿瘤分布多样,组织学也各不相同。我们描述了8例患者(7例女性,1例男性,年龄范围15 - 82岁)的临床病理和分子特征。肿瘤位于卵巢(n = 3)、子宫内膜(n = 1)、腹膜后(n = 1)、皮肤(n = 1)、颈部(n = 1)和下咽(n = 1)。这些病例表现出上皮样(n = 2)、梭形细胞(n = 1)、双相性(n = 1)或圆形细胞(n = 3)形态。后两种肿瘤中有两种具有显著的黏液样基质。一个肿瘤具有多形性且有活跃的有丝分裂活性。免疫组织化学显示S100、全角蛋白AE1/3、EMA、CD56、突触素和嗜铬粒蛋白呈不同程度的阳性。在GLI1扩增的病例中检测到MDM2、CDK4和STAT6的表达。在3个肿瘤中鉴定出融合基因(GLI1::MALAT1,n = 2;PTBP1::GLI2,n = 1)。3例患者存在GLI1扩增,其中2例同时伴有MDM2/CDK4共扩增。1个肿瘤中GLI2扩增。另1例有PTCH1失活突变。通过RNA表达和DNA甲基化谱分析,这些病例形成一个聚类。GLI扩增的肿瘤发生在年龄较大的患者(n = 3)中,这些患者在3 - 27个月内死亡。在年龄较小的患者(n = 3)的肿瘤中鉴定出GLI融合基因和PTCH1突变,这些患者无疾病生存(25 - 31个月)。总之,我们的GLI1/2改变的间叶性肿瘤在RNA水平和表观遗传学上聚类,证实它们形成一个实体,包括具有PTCH1突变的肿瘤。扩增的肿瘤发生在年龄较大的患者中,行为更具侵袭性,而起源于年龄较小患者的具有融合基因的病变预后良好。