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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1959 1
1960 1
1961 1
1963 2
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1965 3
1966 3
1967 3
1968 2
1969 2
1970 5
1971 5
1972 1
1973 7
1974 1
1975 9
1976 6
1977 5
1978 5
1979 5
1980 3
1981 2
1982 4
1983 5
1984 7
1985 3
1986 11
1987 8
1988 10
1989 11
1990 6
1991 10
1992 12
1993 15
1994 5
1995 12
1996 13
1997 14
1998 17
1999 12
2000 16
2001 12
2002 19
2003 7
2004 9
2005 12
2006 17
2007 23
2008 18
2009 26
2010 32
2011 23
2012 34
2013 39
2014 41
2015 44
2016 50
2017 52
2018 45
2019 45
2020 57
2021 48
2022 60
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2024 38
2025 52
2026 38

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1,054 results

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Page 1
Kasabach-Merritt phenomenon.
Kelly M. Kelly M. Pediatr Clin North Am. 2010 Oct;57(5):1085-9. doi: 10.1016/j.pcl.2010.07.006. Epub 2010 Aug 21. Pediatr Clin North Am. 2010. PMID: 20888459 Review.
The objective of this article is to provide a comprehensive overview of the Kasabach-Merritt Phenomenon. The clinical presentation, laboratory findings, vascular pathology, and pathophysiology are discussed....
The objective of this article is to provide a comprehensive overview of the Kasabach-Merritt Phenomenon. The clinical p …
Kasabach-Merritt Phenomenon: Classic Presentation and Management Options.
Mahajan P, Margolin J, Iacobas I. Mahajan P, et al. Clin Med Insights Blood Disord. 2017 Mar 16;10:1179545X17699849. doi: 10.1177/1179545X17699849. eCollection 2017. Clin Med Insights Blood Disord. 2017. PMID: 28579853 Free PMC article. Review.
Kasabach-Merritt phenomenon (KMP) is a rare consumptive coagulopathy associated with specific vascular tumors, kaposiform hemangioendothelioma, and tufted angioma. Kasabach-Merritt phenomenon, characterized by profound thrombocytopenia, h
Kasabach-Merritt phenomenon (KMP) is a rare consumptive coagulopathy associated with specific vascular tumors, kaposifo
Standards of care for Kasabach-Merritt phenomenon in China.
Yao W, Li KL, Qin ZP, Li K, Zheng JW, Fan XD, Ma L, Zhou DK, Liu XJ, Wei L, Li L, Tai MZ, Wang JH, Ji Y, Zhou L, Huang HJ, Gao XY, Huang ZJ, Gu S, Yang HY. Yao W, et al. World J Pediatr. 2021 Apr;17(2):123-130. doi: 10.1007/s12519-020-00379-9. Epub 2020 Aug 26. World J Pediatr. 2021. PMID: 32851561 Review.
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. ...
Kasabach-Merritt phenomenon (KMP) is a rare disease that is characterized by severe thrombocytopenia and consumptive co
Kasabach-Merritt Phenomenon.
Chen YC, Wang TM, Wang JD. Chen YC, et al. J Pediatr. 2015 Nov;167(5):1162. doi: 10.1016/j.jpeds.2015.07.041. Epub 2015 Aug 19. J Pediatr. 2015. PMID: 26298626 No abstract available.
[Kasabach-Merritt phenomenon].
Le Nouail P, Viseux V, Enjolras O; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Le Nouail P, et al. Ann Dermatol Venereol. 2007 Jun-Jul;134(6-7):580-6; quiz 579, 587. doi: 10.1016/s0151-9638(07)89278-7. Ann Dermatol Venereol. 2007. PMID: 17657192 Review. French. No abstract available.
Kaposiform Hemangioendothelioma with Kasabach-Merritt Phenomenon.
Pati S, Das MK, Rana A, Das E, Sarkar S, Sherpa N, Datta S. Pati S, et al. Indian J Pediatr. 2021 Nov;88(11):1142-1144. doi: 10.1007/s12098-021-03817-2. Epub 2021 Jun 9. Indian J Pediatr. 2021. PMID: 34106442
Paradoxical worsening of symptoms with platelet transfusions and radiological evidences led to the diagnosis of a very rare congenital multifocal vascular tumor, kaposiform hemangioendothelioma (KHE) with Kasabach-Merritt phenomenon (KMP). The index case of K …
Paradoxical worsening of symptoms with platelet transfusions and radiological evidences led to the diagnosis of a very rare congenital multi …
Kasabach-Merritt Syndrome.
Famularo G. Famularo G. Am J Med. 2020 Dec;133(12):e747. doi: 10.1016/j.amjmed.2020.02.032. Am J Med. 2020. PMID: 33248667 No abstract available.
Kasabach-Merritt Syndrome.
Lewis D, Vaidya R. Lewis D, et al. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 30085595 Free Books & Documents.
Kasabach-Merritt phenomenon (KMP), first described in 1940, is a rare but life-threatening coagulopathy of infancy which presents with thrombocytopenia, microangiopathic hemolytic anemia, and consumptive coagulopathy in the setting of a rapidly enlarging vasc
Kasabach-Merritt phenomenon (KMP), first described in 1940, is a rare but life-threatening coagulopathy of infancy whic
1,054 results