Soumyaa Gulati, Harsha Gangadhar, Suravi Mohanty, P Shilpashree, Divya Gupta
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引用次数: 0
摘要
血管肉瘤(Angiosarcoma,AS)是一种罕见的血管或淋巴管上皮恶性肿瘤,通常表现为面部或头皮的瘀青样斑块,发病年龄在七十至九十岁之间。在此,我们报告了一例皮肤 AS(cAS)病例,患者为 51 岁男性,腹股沟处长有菜花状赘生物,周围有肤色发亮的平顶卫星丘疹,其中一些呈脐状。根据检查结果,患者被认为是复古阳性,并考虑了以下鉴别因素:布施克-洛温斯坦瘤伴巨型软疣、卡波西肉瘤和鳞状细胞癌。组织病理学检查提示诊断为强直性脊柱炎,免疫组化证实 CD31 和 CD34 阳性。报告强调了 cAS 的不寻常部位和临床表现。
Angiosarcoma (AS) is a rare malignant tumor of vascular or lymphatic epithelium, typically presenting as a bruise-like patch over the face or scalp in the seventh-ninth decades. Here, we report a case of cutaneous AS (cAS) in a 51-year-old male patient who presented with a cauliflower-like growth in the groin with skin-colored shiny flat-topped satellite papules in the surrounding areas, some of which were umbilicated. Based on examination, the patient was considered retro positive and the following differentials were considered: Buschke-Lowenstein tumor with giant molluscum, Kaposi sarcoma, and squamous cell carcinoma. Histopathological examination suggested the diagnosis as AS, which was confirmed by immunohistochemistry that was positive for CD31 and CD34. The report highlights the unusual site and clinical presentation of cAS.