Literature DB >> 23480932

Successful treatment of Kasabach-Merritt syndrome with transarterial embolization and corticosteroids.

Shao-yi Zhou1, Hai-bo Li, Yue-ming Mao, Pei-ying Liu, Jing Zhang.   

Abstract

Kasabach-Merritt syndrome (KMS) refers to the combination of large neonatal vascular tumors and thrombocytopenic coagulopathy. However, a standard treatment regimen for KMS has not yet been established. We report a case of a 6-week-old male infant with life-threatening KMS who was successfully treated with transarterial embolization and corticosteroids. One week after initiating the corticosteroid treatment, his platelet counts recovered, and the lesion growth halted. The approach with corticosteroid therapy resulted in an excellent response that was maintained long enough for us to perform transarterial embolization therapy. The combination of transarterial embolization and corticosteroid therapy should be considered as an option for Kasabach-Merritt syndrome.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23480932     DOI: 10.1016/j.jpedsurg.2012.12.049

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  6 in total

1.  Kasabach-Merritt phenomenon in a neonatal kaposiform haemangioendothelioma.

Authors:  Veronica Mardegan; Nicoletta Doglioni; Giuseppe De Bernardo; Daniele Trevisanuto
Journal:  BMJ Case Rep       Date:  2014-08-12

2.  Case Report: Congenital Intracranial Kaposiform Hemangioendothelioma Treated With Surgical Resection.

Authors:  Yingjie Cai; Jiayi Li; Wei Yang; Nan Zhang; Hailang Sun; Weiping Zhang; Ming Ge
Journal:  Front Surg       Date:  2022-04-01

3.  Successful management of steroid-resistant vascular tumors associated with the Kasabach-Merritt phenomenon using sirolimus.

Authors:  Xiaoyun Tan; Jing Zhang; Shaoyi Zhou; Zhenyin Liu; Tao Zhang; Jiejun Xia
Journal:  J Dermatol       Date:  2018-01-21       Impact factor: 4.005

4.  Effective surgical treatment of life-threatening huge vascular anomalies associated with thrombocytopenia and coagulopathy in infants unresponsive to drug therapy.

Authors:  Yaohao Wu; Ronglin Qiu; Lexiang Zeng; Liyang Liang; Jie Zhang; Jiajia Zhou; Wenli Jiang; Jianhang Su; Xiaogeng Deng
Journal:  BMC Pediatr       Date:  2020-04-27       Impact factor: 2.125

5.  Analysis of angiographic characteristics of kaposiform hemangioendothelioma and investigation of the value of transcatheter arterial embolization therapy.

Authors:  Xiaoyun Tan; Zhenyin Liu; Shaoyi Zhou; Kunshan Chen; Ming Zhang; Jiejun Xia; Yiqun Guo; Zijun Zhou
Journal:  Transl Pediatr       Date:  2021-12

6.  Effective low-dose sirolimus regimen for kaposiform haemangioendothelioma with Kasabach-Merritt phenomenon in young infants.

Authors:  Veroniek E M Harbers; Nathalie van der Salm; Sjoert A H Pegge; Carine J M van der Vleuten; Bas H Verhoeven; Sabine L A G Vrancken; Leo J Schultze Kool; Joris Fuijkschot; D Maroeska M W M Te Loo
Journal:  Br J Clin Pharmacol       Date:  2022-01-18       Impact factor: 3.716

  6 in total

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