Liang D, Zhou B, Li N, Kong L F, Liu Q Y, Ding K L, Niu X S, Zhu H H, Zhu Haohui
Department of Breast Surgery, Henan Provincial People's Hospital, Zhengzhou 450003, China.
Department of Pathology, Weishi People's Hospital, Kaifeng 475000, China.
Zhonghua Bing Li Xue Za Zhi. 2022 Mar 8;51(3):202-206. doi: 10.3760/cma.j.cn112151-20211026-00776.
To investigate the clinical and pathologic features, diagnosis and differential diagnosis of congenital hemangioma (CH). Forty cases of CH were diagnosed from January 2017 to December 2020 in Henan Provincial People's Hospital. The clinical and pathological and immunohistochemical data were analyzed, with review of literature. There were 24 male and 16 female patients. The lesions were located in the head, neck (11 cases), limbs (14 cases), and trunk (15 cases). The clinical manifestations were congenital painless plaques or masses, the larger ones protruded on the skin surface, mostly dusky purple or bright red, with surrounding white halos. Under low magnification, the tumor was lobular and well demarcated, composed of neo-microvascular lumen of different sizes. The vascular endothelial cells were cuboidal or hobnail in appearance, forming stellar drainage vessels within the lobules. Extra-medullary hematopoiesis was seen in one case of rapidly involuting CH; there were different number of tortuous and dilated vascular lumen between the lobular structures, and some non-involuting CH cases were vascular malformations, which were devoid of lobulated structures. Immunohistochemistry showed that endothelial cells were strongly positive for CD31, CD34 and ERG, while D2-40 and GLUT-1 were negative. CH is a benign congenital vascular tumor with characteristic lobulated growth and abnormal blood vessels in the stroma. Pathological diagnosis often needs to be differentiated from infantile hemangioma, pyogenic granuloma, kaposiform hemangioendothelioma and vascular malformation.
探讨先天性血管瘤(CH)的临床及病理特征、诊断与鉴别诊断。回顾性分析2017年1月至2020年12月在河南省人民医院诊断的40例CH患者的临床、病理及免疫组化资料,并复习相关文献。患者中男性24例,女性16例。病变位于头颈部11例、四肢14例、躯干15例。临床表现为先天性无痛性斑块或肿块,较大者突出于皮肤表面,多为暗紫色或鲜红色,周围有白色晕圈。低倍镜下,肿瘤呈小叶状,边界清晰,由大小不等的新生微血管腔组成。血管内皮细胞呈立方形或鞋钉样,在小叶内形成星状引流血管。1例快速消退型CH可见髓外造血;小叶结构之间有数量不等的迂曲扩张血管腔,部分非消退型CH病例为血管畸形,无小叶状结构。免疫组化显示,内皮细胞CD31、CD34和ERG呈强阳性,而D2-40和GLUT-1呈阴性。CH是一种良性先天性血管肿瘤,具有特征性的小叶状生长及间质内异常血管。病理诊断常需与婴儿血管瘤、化脓性肉芽肿、卡波西样血管内皮瘤及血管畸形相鉴别。