Das Kapil Dev, Ghosh Kaushik, Kar Chinmoy, Gharami Ramesh Chandra, Chakraborty Sisir, Bhattacharyya Ambarish
Department of Dermatology, Malda Medical College, Burdwan, West Bengal, India.
Malda and Department of Medicine, Burdwan Medical College, Burdwan, West Bengal, India.
Indian J Dermatol. 2015 Sep-Oct;60(5):509-11. doi: 10.4103/0019-5154.159664.
Spindle-cell hemangioendothelioma (SCHE) comprise a rare subset of vascular tumors, and here, we describe such a case and review the clinical presentation, patho-physiology, differential diagnosis of these tumors to promote early identification and discussion guidance. A 25-years-old male patient presented with multiple painful elevated swellings of both left upper and lower extremities for last 15 years without any systemic involvement. After excluding close differential diagnosis by relevant investigations an excisional biopsy was performed. Based on clinical, radiological and histopathological findings, diagnosis of SCHE was made and full thickness excision and skin grafting were performed. The case is reported due to its rarity and adds our knowledge to the existing literature.
梭形细胞血管内皮瘤(SCHE)是血管肿瘤中罕见的一个亚型,在此,我们描述这样一例病例,并回顾这些肿瘤的临床表现、病理生理学及鉴别诊断,以促进早期识别并提供讨论指导。一名25岁男性患者,在过去15年里双侧上肢和下肢出现多处疼痛性隆起肿胀,无任何全身受累情况。经相关检查排除相近的鉴别诊断后,进行了切除活检。根据临床、放射学和组织病理学检查结果,诊断为SCHE,并进行了全层切除和植皮。该病例因其罕见性而被报道,为现有文献增添了我们的知识。