| Literature DB >> 32851561 |
Wei Yao1, Ke-Lei Li2, Zhong-Ping Qin3, Kai Li1, Jia-Wei Zheng4, Xin-Dong Fan5, Lin Ma6, De-Kai Zhou7, Xue-Jian Liu8, Li Wei6, Li Li6, Mao-Zhong Tai2, Jin-Hu Wang9, Yi Ji10, Lin Zhou11, Hai-Jin Huang12, Xiao-Yun Gao13, Zhi-Jian Huang14, Song Gu15, He-Ying Yang16.
Abstract
Kasabach-Merritt phenomenon (KMP) is a rare disease that is characterized by severe thrombocytopenia and consumptive coagulation dysfunction caused by kaposiform hemangioendothelioma or tufted hemangioma. This condition primarily occurs in infants and young children, usually with acute onset and rapid progression. This review article introduced standardized recommendations for the pathogenesis, clinical manifestation, diagnostic methods and treatment process of KMP in China, which can be used as a reference for clinical practice.Entities:
Keywords: Kaposiform hemangioendothelioma; Kasabach−Merritt phenomenon; Tufted hemangioma
Year: 2020 PMID: 32851561 DOI: 10.1007/s12519-020-00379-9
Source DB: PubMed Journal: World J Pediatr Impact factor: 2.764