Shinkai Toko, Masumoto Kouji, Ono Kentaro, Yano Eri, Kobayashi Chie, Fukushima Takashi, Sumazaki Ryo, Satomi Kaishi, Noguchi Masayuki
Department of Pediatric Surgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Surg Case Rep. 2015 Dec;1(1):42. doi: 10.1186/s40792-015-0042-4. Epub 2015 May 16.
Lipoblastoma, a relatively rare benign adipose neoplasm, predominantly affects children younger than 3 years of age. We herein report the case of a 7-month-old girl with an unusual myxomatous histology of lipoblastoma. A rapidly growing mass was detected in the subcutaneous area of the left buttock. Histologically, the tumor consisted of abundant myxoid stroma exhibiting cellular atypia and a high mitotic activity. Although the histological findings were unusual, the tumor was diagnosed as a lipoblastoma according to both PLAG1 immunohistochemistry and the presence of PLAG1 rearrangement on fluorescence in situ hybridization.
脂肪母细胞瘤是一种相对罕见的良性脂肪肿瘤,主要影响3岁以下的儿童。我们在此报告一例7个月大女童患有一种不寻常的黏液样组织学类型的脂肪母细胞瘤。在左臀部皮下区域检测到一个快速生长的肿块。组织学上,肿瘤由丰富的黏液样间质组成,表现出细胞异型性和高有丝分裂活性。尽管组织学表现不寻常,但根据PLAG1免疫组化以及荧光原位杂交检测到的PLAG1重排,该肿瘤被诊断为脂肪母细胞瘤。