Ozaki Yukinori, Miura Yuji, Koganemaru Shigehiro, Suyama Koichi, Inoshita Naoko, Fujii Takeshi, Hashimoto Masaji, Tamura Tetsuo, Takeuchi Kazuo, Takano Toshimi
Department of Medical Oncology, Toranomon Hospital, 2-2-2 Toranomon, Minato-ku, Tokyo, 105-8470, Japan.
Department of Pathology, Toranomon Hospital, Tokyo, Japan.
BMC Cancer. 2015 Jan 22;15:16. doi: 10.1186/s12885-015-1017-3.
Ewing sarcoma is a rare tumor that occurs commonly in the long bones of children or adolescents that can also arise in soft tissues including the extremities, retroperitoneum, chest wall, and rarely in the liver as primary sites. We report a case of Ewing sarcoma arising primarily in the liver and, to our knowledge, this is the fourth reported case of Ewing sarcoma occurring in the liver.
A 27-year-old Japanese woman was admitted with sudden onset right upper abdominal pain. Clinical examination revealed a multilocular cystic mass consisting of thickened, irregular septa and nodal walls in the right hepatic lobe. Ultrasound-guided aspiration biopsy of the liver mass showed clusters of small atypical round cells and the clinical preoperative diagnosis was mucinous cystadenoma of the liver. The patient underwent an extended right hepatectomy and histopathological findings revealed sheet-like proliferation of small- to medium-sized round cells. Tumor cells were positive for periodic acid-Schiff reaction and immunoreactive for glycoprotein C99 and gene NKX2.2, as well as the neuroendocrine markers, CD56 and synaptophysin. EWS-FLI-1 fusion transcript type 1 was detected by reverse transcriptase polymerase chain reaction. Pathological and molecular analysis confirmed the diagnosis of Ewing sarcoma arising primarily in the liver and the patient received adjuvant systemic chemotherapy with vincristine, doxorubicin, and cyclophosphamide, alternating with ifosfamide and etoposide. We found no evidence of recurrence 15 months after completing chemotherapy.
We present an extremely rare case of Ewing sarcoma arising primarily in the liver. To our knowledge, this is the fourth reported case of Ewing sarcoma occurring in the liver, and the first case with a multilocular cystic liver mass. Imaging examinations of the other three reported cases showed solid tumors and a diffuse enlarged liver without mass lesion. Clinicians should consider the possibility of Ewing sarcoma in young patients with a multilocular cystic mass with thick and/or irregular cyst walls in the liver.
尤因肉瘤是一种罕见肿瘤,常见于儿童或青少年的长骨,也可发生于包括四肢、腹膜后、胸壁等软组织,极少以肝脏作为原发部位。我们报告一例主要发生于肝脏的尤因肉瘤病例,据我们所知,这是第四例报道的发生于肝脏的尤因肉瘤病例。
一名27岁日本女性因突发右上腹疼痛入院。临床检查发现右肝叶有一个多房性囊性肿块,由增厚、不规则的间隔和囊壁组成。肝脏肿块的超声引导下穿刺活检显示有小的非典型圆形细胞簇,临床术前诊断为肝脏黏液性囊腺瘤。患者接受了扩大右肝切除术,组织病理学检查发现中小圆形细胞呈片状增生。肿瘤细胞过碘酸希夫反应阳性,对糖蛋白C99和基因NKX2.2以及神经内分泌标志物CD56和突触素免疫反应阳性。通过逆转录聚合酶链反应检测到EWS-FLI-1融合转录本1型。病理和分子分析证实诊断为主要发生于肝脏的尤因肉瘤,患者接受了长春新碱、阿霉素和环磷酰胺辅助全身化疗,与异环磷酰胺和依托泊苷交替使用。完成化疗15个月后,我们未发现复发迹象。
我们报告了一例极为罕见的主要发生于肝脏的尤因肉瘤病例。据我们所知,这是第四例报道的发生于肝脏的尤因肉瘤病例,也是第一例有多房性囊性肝脏肿块的病例。其他三例报道病例的影像学检查显示为实性肿瘤和弥漫性肝脏肿大且无肿块病变。临床医生应考虑到年轻患者肝脏出现多房性囊性肿块且囊壁增厚和/或不规则时尤因肉瘤的可能性。