Gong Qi-xing, Fan Qin-he, Xie Jun, Su Zhong-lan, Zhang Mei-hua, Zhang Zhi-hong
Department of Pathology, First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
Zhonghua Bing Li Xue Za Zhi. 2013 Sep;42(9):593-8.
To study the clinicopathologic features, diagnosis and differential diagnosis of epithelioid hemangioma.
The morphologic features of 7 cases of epithelioid hemangioma of skin, bone and venous vessels were studied.
There were altogether 4 male and 3 female patients (median age = 34 years; age range from 14 to 54 years). The 3 skin cases presented as single or multiple erythematous to bluish nodules or papules, with or without itchiness. The 2 bone cases appeared as osteolytic expansile lesions on radiologic examination. The remaining 2 cases involved medium-sized venous structures and presented as small isolated nodules in soft tissue. Histologically, the lesions were characterized by the presence of exuberant endothelial proliferations with various degree of inflammatory reaction. The neoplastic endothelial cells were plump, eosinophilic and polygonal, forming vascular channels. Occasional solid sheet-like arrangement was demonstrated. Intracytoplasmic vacuoles were commonly identified, indicating formation of primary lumen. The surrounding stroma contained various number of eosinophils and lymphoplasmacytic cells. Immunohistochemical study showed that the tumor cells were positive for endothelial markers (CD31 and CD34) and negative for epithelial marker (cytokeratin). Follow-up information was available in 6 cases. The duration of follow-up ranged from 5 to 36 months (median = 14 months). There was no evidence of recurrence or distant metastasis.
Epithelioid hemangioma is a rare benign curable lesion which can be multifocal, involving skin, soft tissue and bone. It needs to be distinguished from Kimura's disease and epithelioid hemangioendothelioma.
研究上皮样血管瘤的临床病理特征、诊断及鉴别诊断。
对7例皮肤、骨及静脉血管上皮样血管瘤的形态学特征进行研究。
患者共4例男性和3例女性(中位年龄 = 34岁;年龄范围14至54岁)。3例皮肤病例表现为单个或多个红斑至蓝色结节或丘疹,伴或不伴瘙痒。2例骨病例在影像学检查中表现为溶骨性膨胀性病变。其余2例累及中等大小静脉结构,表现为软组织内孤立小结节。组织学上,病变特征为内皮细胞显著增生并伴有不同程度的炎症反应。肿瘤性内皮细胞饱满、嗜酸性、多边形,形成血管腔隙。偶尔可见实性片状排列。胞质内空泡常见,提示原始管腔形成。周围间质含有数量不等的嗜酸性粒细胞和淋巴浆细胞。免疫组化研究显示肿瘤细胞内皮标志物(CD31和CD34)阳性,上皮标志物(细胞角蛋白)阴性。6例有随访信息。随访时间为5至36个月(中位 = 14个月)。无复发或远处转移证据。
上皮样血管瘤是一种罕见的可治愈的良性病变,可多灶性发生,累及皮肤、软组织和骨。需与木村病和上皮样血管内皮瘤相鉴别。