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首页> 外文期刊>Indian Dermatology Online Journal >Congenital infiltrating lipomatosis of the face: A case report with review of literature
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Congenital infiltrating lipomatosis of the face: A case report with review of literature

机译:先天性面部浸润性脂肪瘤:一例报道并文献复习

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Congenital infiltrating lipomatosis of the face (CIL-F) has been described as a disorder in which mature lipocytes invade adjacent tissues in the facial region. Its etiology and pathogenesis is unknown. The tumor is congenital in origin and occurs in infancy or early childhood. It is unencapsulated and characterized by diffuse infiltration of mature adipose tissue over normal muscle fibers, rapid growth, associated osseous hyperplasia, and a high recurrence rate postsurgical intervention. Due to its diffuse infiltration and involvement of important facial structures, complete surgical excision is often impossible. CIL-F is rare and there are only a few cases reported in the available literature. We present the case of a 17-year-old female, who reported with the complaint of recurrent unilateral facial swelling, with a history of two previous resections.Keywords: Face, lipomatosis, nevus, recurrence
机译:先天性面部浸润性脂肪瘤病(CIL-F)被描述为一种疾病,其中成熟的脂肪细胞侵入面部区域的相邻组织。其病因和发病机理未知。肿瘤起源于先天性,发生在婴儿期或儿童早期。它没有被封装,其特征是成熟脂肪组织在正常的肌肉纤维上扩散浸润,生长迅速,伴有骨性增生以及术后复发率高。由于其弥漫性浸润和重要的面部结构受累,通常不可能进行完全的手术切除。 CIL-F很少见,现有文献仅报道了少数病例。我们报道了一名17岁女性的病例,该女性因抱怨复发性单侧面部肿胀而有两次切除的历史。关键词:面部,脂肪过多,痣,复发

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