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.
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YW and LKL contributed equally to this paper. They design, acquisition, analysis and draft the manuscript; QZP contributed to conception, design, acquisition data of the manuscript; LK contributed to conception, design, acquisition data of the manuscript; ZJW contributed to conception, design, acquisition data of the manuscript; FXD contributed to revise the manuscript contributed to acquisition data of the manuscript; ML contributed to analysis and interpretation of data and revise the manuscript; ZDK contributed to analysis and interpretation of data and revise the manuscript; LXJ contributed to acquisition data of the manuscript; WL contributed to acquisition data of the manuscript; LL contributed to acquisition data of the manuscript; TMZ contributed to acquisition data of the manuscript; WJH contributed to acquisition data of the manuscript; JY contributed to analysis and interpretation of data; ZL contributed to analysis and interpretation of data; HHJ contributed to analysis and interpretation of data; GXY contributed to analysis and interpretation of data; HZJ contributed to analysis and interpretation of data; GS contributed to analysis and interpretation of data; YHY contributed to analysis and interpretation of data.
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Yao, W., Li, KL., Qin, ZP. et al. Standards of care for Kasabach−Merritt phenomenon in China. World J Pediatr 17, 123–130 (2021). https://doi.org/10.1007/s12519-020-00379-9
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DOI: https://doi.org/10.1007/s12519-020-00379-9