摘要
目的了解脂肪纤维瘤病的临床病理。方法收集4例脂肪纤维瘤病临床资料,手术切除组织光镜切片观察,另作4项免疫组织化学单克隆标记,SMA,S100蛋白,Vimentin,Desmin。结果3例为出生不久就发现肿块,1例为12岁。肿瘤1例位于左侧颞部眉弓下,3例位于躯干部。肿瘤由纤维组织和脂肪组织构成。免疫组织化学标记瘤组织S100蛋白和Vimentin阳性,SMA和Desmin阴性。结论脂肪纤维瘤病是一种罕见的肿瘤,它的诊断依靠病理组织学改变和免疫组织化学标记,肿瘤可多发和复发。
Obioctive To investigate the clinicopathological features of lipofibromatosis. Methods By means of histological, and immunohistochemical studies, the clinical and pathological features of four cases of lipofibromatosis were analyzed. Results The patients of first two cases were girl 2 and 12 year old, cases 3 was a femal 25year old, case 4 was a male 15 year tumors were located in the right gluteal and ventralis anterior, below of left arcus superciliaris, sacroiliac. S100 protin, were positive and SMA and desemin was negative ia the tumor. Conclusion The lipofibromatosis is a rare tumor. The is based on histological, immunohistochemical staining.
出处
《罕少疾病杂志》
2009年第4期6-8,共3页
Journal of Rare and Uncommon Diseases
关键词
婴儿
脂肪纤维瘤病
免疫组织化学
组织学
lipofibromatosis, himmunohistochemistry
microscopy old. The Vimentin diagnosis
