Jiahua Xing , Yi Chen , Liwu Zheng , Yan Shao , Yichi Xu , Lingli Guo
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引用次数: 1
Abstract
Dermatofibromas are benign soft tissue tumors that predominantly affect the limbs, and more rarely the chest. Keloidal dermatofibroma is a rare subtype with distinct clinicopathological features and an aggressive clinical course. By researching the evolution of the disease in this study, we aimed to summarize our experience of managing a rare patient who underwent five surgeries for keloidal dermatofibroma that developed sequentially in the upper arm and chest and propose a novel treatment for keloidal dermatofibroma. We concluded that keloidal dermatofibroma involving larger areas, high tension sites, and multiple localizations can be treated using the principles of pathological scar management.