Tsukamoto Yoshitane, Futani Hiroyuki, Yoshiya Shinichi, Watanabe Takahiro, Kihara Takako, Matsuo Shohei, Hirota Seiichi
Department of Surgical Pathology, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan; Department of Pathology and Laboratory Medicine, Takarazuka City Hospital, 4-5-1 Kohama, Takarazuka, Hyogo 665-0827, Japan.
Department of Orthopaedic Surgery, Hyogo College of Medicine, Nishinomiya, Japan.
Pathol Res Pract. 2017 Oct;213(10):1315-1321. doi: 10.1016/j.prp.2017.06.008. Epub 2017 Jun 6.
We experienced a 38-year-old Japanese male with t(10;19) CIC-DUX4 -positive undifferentiated small round cell sarcoma in the deep abdominal wall. Three months before his first visit to our hospital, he noticed a mass in his right abdominal wall. Computed tomography on admission revealed a solid abdominal tumor 70×53mm in size and multiple small tumors in both lungs. The biopsy of the abdominal tumor revealed undifferentiated small round cell sarcoma, suggestive of Ewing sarcoma. Under the clinical diagnosis of Ewing-like sarcoma of the abdominal wall with multiple lung metastases, several cycles of ICE (ifosfamide, carboplatin and etoposide) therapy were performed. After the chemotherapy, the lung metastases disappeared, while the primary lesion rapidly grew. Additional VDC (vincristine, doxorubicin and cyclophosphamide) therapy was carried out without apparent effect. Although the surgical removal of the primary lesion was done, peritoneal dissemination and a huge metastatic liver tumor appeared thereafter. The patient died of disease progression two months after the surgery. The total clinical course was approximately one year, showing that the tumor was extremely aggressive. The tumor cells of the surgical specimen were positive for CD99, WT1, calretinin, INI1, ERG and Fli1 by immunohistochemistry. Fusion gene analyses using the frozen surgical material revealed negativity for EWSR1-Fli1, EWSR1-ERG and t(4;19) CIC-DUX4 fusions, but positivity for t(10;19) CIC-DUX4 fusion. Thus, we made a final pathological diagnosis of t(10;19) CIC-DUX4-positive undifferentiated small round cell sarcoma. To our knowledge, this is the 13th case of t(10;19) CIC-DUX4 undifferentiated small round cell sarcoma with precise clinicopathological information. Especially in our case, two types of t(10;19) CIC-DUX4 fusion transcripts were observed, both of which are in-frame and novel.
我们接诊了一名38岁的日本男性,其腹壁深部患有t(10;19) CIC-DUX4阳性的未分化小圆形细胞肉瘤。在他首次来我院就诊前三个月,他发现右腹壁有一个肿块。入院时的计算机断层扫描显示,腹部有一个大小为70×53mm的实性肿瘤,双肺有多个小肿瘤。腹部肿瘤活检显示为未分化小圆形细胞肉瘤,提示尤因肉瘤。在临床诊断为腹壁尤因样肉瘤伴多发肺转移后,进行了几个周期的ICE(异环磷酰胺、卡铂和依托泊苷)治疗。化疗后,肺转移灶消失,但原发灶迅速增大。随后进行了VDC(长春新碱、阿霉素和环磷酰胺)治疗,但无明显效果。尽管对原发灶进行了手术切除,但此后出现了腹膜播散和巨大的肝转移瘤。患者术后两个月因疾病进展死亡。整个临床病程约为一年,表明肿瘤极具侵袭性。手术标本的肿瘤细胞经免疫组织化学检测,CD99、WT1、钙视网膜蛋白、INI1、ERG和Fli1呈阳性。使用冷冻手术材料进行融合基因分析显示,EWSR1-Fli1、EWSR1-ERG和t(4;19) CIC-DUX4融合均为阴性,但t(10;19) CIC-DUX4融合为阳性。因此,我们最终做出了t(10;19) CIC-DUX4阳性未分化小圆形细胞肉瘤的病理诊断。据我们所知,这是第13例具有精确临床病理信息的t(10;19) CIC-DUX4未分化小圆形细胞肉瘤。特别是在我们的病例中,观察到两种类型的t(10;19) CIC-DUX4融合转录本,均为框内且新颖。