| Literature DB >> 17581327 |
Zhaoyue Wang1, Ziqiang Yu, Yanhua Su, Haiyan Yang, Lijuan Cao, Xiaojuan Zhao, Hao Hu, Shenghua Zhan, Changgeng Ruan.
Abstract
Proteus syndrome is a rare hamartomous disorder with highly variable manifestations of disproportionate overgrowth of body parts, epidermal nevi and vascular malformations. We describe two patients who had typical clinical and imaging Proteus syndrome features. One of most characteristic findings in these two patients was that they had giant hemangiomas of the spleen that caused Kasabach-Merritt syndrome, demonstrating clinical bleeding and disseminated intravascular coagulation laboratory alterations. The present two cases are the first report of this complication in Proteus syndrome. The patients' bleeding tendency and hemostatic defects were completely corrected after they successfully underwent splenectomy.Entities:
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Year: 2007 PMID: 17581327 DOI: 10.1097/MBC.0b013e32814203af
Source DB: PubMed Journal: Blood Coagul Fibrinolysis ISSN: 0957-5235 Impact factor: 1.276