Sumida Satoshi, Toki Shun-Ichi, Mori Taisuke, Satomi Kaishi, Takao Shoichiro, Nobusawa Sumihito, Kakimoto Takumi, Nakagawa Shinya, Ryo Eijitsu, Matsushita Yuko, Ichimura Koichi, Nishisho Toshihiko, Bando Yoshimi, Yoshida Akihiko
Division of Pathology, Tokushima University Hospital, Tokushima, Japan.
Department of Orthopedics, Institute of Biomedical Sciences, Tokushima University, Tokushima, Japan.
Genes Chromosomes Cancer. 2023 Feb;62(2):101-106. doi: 10.1002/gcc.23098. Epub 2022 Oct 19.
Chondroid lipoma is a rare benign adipose tumor characterized by a recurrent ZFTA::MRTFB fusion. Herein, we report an unusual liposarcoma that partly exhibited overlapping features with those of chondroid lipoma and harbored a ZFTA::RELA fusion. A 59-year-old man presented with a shoulder mass that had existed for approximately 8 years and with increasing pain due to a pelvic mass. The 5.8-cm resected shoulder tumor partly consisted of nests and strands of variably lipogenic epithelioid cells within a hyalinized or focally chondromyxoid stroma, indistinguishable from chondroid lipoma. The histological pattern gradually transitioned to highly cellular, stroma-poor, diffuse sheets of cells with greater nuclear atypia and mitotic activity. Vascular invasion and necrosis were present. The metastatic pelvic tumor revealed a similar histology. Despite multimodal treatment, the patient developed multiple bone metastases and succumbed to the disease 14 months after presentation. Targeted RNA sequencing identified an in-frame ZFTA (exon 3)::RELA (exon 2) fusion, which was confirmed by reverse transcription-polymerase chain reaction, Sanger sequencing, and break-apart fluorescent in situ hybridization assays. The tumor showed a different histology from that of ependymoma, no brain involvement, and no match with any sarcoma types or ZFTA::RELA-positive ependymomas according to DNA methylation analysis. p65 and L1CAM were diffusely expressed, and a CDKN2A/B deletion was present. This is the first report of an extra-central nervous system tumor with a ZFTA::RELA fusion. The tumor partly displayed an overlapping histology with that of chondroid lipoma, suggesting that it may represent a hitherto undescribed malignant chondroid lipoma with an alternative ZFTA fusion.
软骨样脂肪瘤是一种罕见的良性脂肪肿瘤,其特征为反复出现的ZFTA::MRTFB融合。在此,我们报告一例不寻常的脂肪肉瘤,其部分表现出与软骨样脂肪瘤重叠的特征,并含有ZFTA::RELA融合。一名59岁男性患者,肩部肿物存在约8年,因盆腔肿物导致疼痛加剧。切除的5.8 cm肩部肿瘤部分由透明变性或局灶性软骨黏液样基质内的巢状和条索状不同程度脂肪生成的上皮样细胞组成,与软骨样脂肪瘤难以区分。组织学模式逐渐转变为细胞丰富、基质少的弥漫性细胞片,核异型性和有丝分裂活性增加。存在血管侵犯和坏死。转移性盆腔肿瘤显示出类似的组织学特征。尽管进行了多模式治疗,患者仍发生多处骨转移,并在就诊后14个月死于该疾病。靶向RNA测序鉴定出一个读码框内的ZFTA(外显子3)::RELA(外显子2)融合,通过逆转录-聚合酶链反应、桑格测序和断裂分离荧光原位杂交分析得以证实。根据DNA甲基化分析,该肿瘤显示出与室管膜瘤不同的组织学特征,无脑部受累,也与任何肉瘤类型或ZFTA::RELA阳性室管膜瘤不匹配。p65和L1CAM弥漫性表达,且存在CDKN2A/B缺失。这是首例报道的具有ZFTA::RELA融合的中枢神经系统外肿瘤。该肿瘤部分显示出与软骨样脂肪瘤重叠的组织学特征,提示它可能代表一种迄今未描述的具有替代ZFTA融合的恶性软骨样脂肪瘤。