Ishikawa Akira, Kuraoka Kazuya, Zaitsu Junichi, Saito Akihisa, Kamigaichi Atsushi, Mimura Takeshi, Yamashita Yoshinori, Taniyama Kiyomi
Department of Clinical Laboratory, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Kure, Japan.
Department of Diagnostic Pathology, National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Kure, Japan.
Case Rep Oncol. 2021 Feb 25;14(1):101-106. doi: 10.1159/000509772. eCollection 2021 Jan-Apr.
Primary mediastinal sarcomas are extremely rare. Additionally, mediastinal leiomyosarcomas account for approximately 9% of mediastinal sarcoma cases. Until date, only few cases of anterior mediastinal leiomyosarcomas have been reported. Herein, we report a case of an 85-year-old female with an anterior mediastinal mass of 15 mm. Histological examination revealed spindle tumor cells showing a fascicular growth pattern. Immunohistochemically, the tumor cells were focal positive for desmin, calponin, and α-smooth muscle actin. The pathological diagnosis was leiomyosarcoma. In conclusion, we encountered a case of a very rare leiomyosarcoma that occurred in the anterior mediastinum, and our report may contribute to the understanding of this disease.
原发性纵隔肉瘤极为罕见。此外,纵隔平滑肌肉瘤约占纵隔肉瘤病例的9%。迄今为止,仅有少数前纵隔平滑肌肉瘤病例被报道。在此,我们报告一例85岁女性,其前纵隔有一个15毫米的肿块。组织学检查显示梭形肿瘤细胞呈束状生长模式。免疫组化结果显示,肿瘤细胞对结蛋白、钙调蛋白和α-平滑肌肌动蛋白呈局灶性阳性。病理诊断为平滑肌肉瘤。总之,我们遇到了一例发生在前纵隔的非常罕见的平滑肌肉瘤病例,我们的报告可能有助于对该疾病的认识。