Department of Pathology and Laboratory Medicine, Dartmouth Health Medical Center, Lebanon, New Hampshire, USA.
Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.
Genes Chromosomes Cancer. 2024 Nov;63(11):e70015. doi: 10.1002/gcc.70015.
Conventional high-grade osteosarcomas are characterized by aggressive radiologic features, cytologic pleomorphism, and complex genomics. However, rare examples of osteosarcomas remain challenging due to unusual histology, such as sclerosing or osteoblastoma-like features, which may require molecular confirmation of their complex genetic alterations. We have encountered such a case in a 17-year-old man, who presented with a third metatarsal sclerotic bone lesion, found incidentally in the work-up of a foot trauma. The initial imaging revealed a lesion with sclerotic/blastic features proximally and lucent/lytic portion distally, findings interpreted consistent with osteoblastoma. The lesion was managed intra-lesionally with curettings and cryoablation; however, the microscopic findings were non-specific, showing a bland osteoblastic proliferation embedded in a densely sclerotic matrix. Subsequently, the patient developed two rapid recurrences; the first recurrence was treated similarly despite its associated soft tissue extension radiographically, and the histologic findings remained non-specific. The 2nd recurrence showed a large mass, with bone destruction and soft tissue extension and an open biopsy revealed features of osteosarcoma with lace-like osteoid deposition, albeit with uniform cytomorphology. The subsequent below knee amputation showed features compatible with high-grade osteosarcoma, including solid growth of uniform epithelioid cells, with vesicular nuclei and scant cytoplasm, set in a lace-like meshwork of osteoid matrix. There was significant mitotic activity and tumor necrosis. Tumor cells were positive for SATB2. Further molecular work-up was performed showing an unexpected NIPBL::BEND2 fusion, which has been previously reported in two cases of phosphaturic mesenchymal tumor (PMT). FGF23 (ISH) was performed and was negative. By DNA methylation profiling, unsupervised clustering and UMAP dimensionality reduction revealed grouping with high-grade osteosarcomas and not with the PMT group. The patient received chemotherapy post-amputation and is alive without evidence of disease, with 10-month follow-up. We report an aggressive, overtly malignant acral bone-forming tumor, harboring a NIPBL::BEND2 fusion. Further studies are needed to evaluate the recurrent potential of this fusion in osteosarcomas and its relationship with PMT.
传统的高级别骨肉瘤具有侵袭性的影像学特征、细胞学多形性和复杂的基因组学。然而,由于罕见的组织学表现,如硬化或骨母细胞瘤样特征,某些骨肉瘤仍然具有挑战性,这可能需要分子方法确认其复杂的遗传改变。我们遇到了这样一个病例,一名 17 岁男性因足部创伤接受检查时偶然发现第三跖骨硬化性骨病变。最初的影像学表现为病变近端硬化/成骨特征和远端透亮/溶骨性部分,这一表现与骨母细胞瘤一致。病变采用刮除和冷冻消融进行腔内治疗;然而,显微镜下的表现是非特异性的,表现为嵌入致密硬化基质中的温和成骨细胞增生。随后,患者出现两次快速复发;尽管第一次复发伴有放射学上的软组织延伸,但仍采用类似的方法进行治疗,其组织学表现仍然是非特异性的。第二次复发表现为一个大肿块,伴有骨破坏和软组织延伸,开放性活检显示出骨肉瘤的特征,伴有花边状骨样沉积,尽管细胞形态均匀。随后的膝下截肢显示出与高级别骨肉瘤一致的特征,包括均匀上皮样细胞的实性生长,具有泡状核和稀少的细胞质,设置在花边状骨样基质的网眼中。有明显的有丝分裂活性和肿瘤坏死。肿瘤细胞 SATB2 阳性。进一步的分子检测显示出意外的 NIPBL::BEND2 融合,之前已有两例报道为磷酸盐尿性间叶肿瘤(PMT)。进行了 FGF23(ISH)检测,结果为阴性。通过 DNA 甲基化谱分析,无监督聚类和 UMAP 降维显示与高级别骨肉瘤聚类,而不是与 PMT 组聚类。患者截肢后接受化疗,目前无疾病证据,随访 10 个月。我们报告了一种侵袭性的、明显恶性的肢端骨形成肿瘤,携带 NIPBL::BEND2 融合。需要进一步的研究来评估这种融合在骨肉瘤中的复发潜力及其与 PMT 的关系。