Literature DB >> 20730884

Treatment of childhood kaposiform hemangioendothelioma with sirolimus.

Julie Blatt1, Joseph Stavas, Billie Moats-Staats, John Woosley, Dean S Morrell.   

Abstract

Sirolimus (Rapamune), a mammalian target of Rapamycin (mTOR) inhibitor, which has been used extensively in children following solid organ transplantation, has been demonstrated to have anti-angiogenic activity in pre-clinical models. Limited experience suggests that it may have application to the treatment of vascular lesions. We describe our experience with a 1-year-old female with a kaposiform hemangioendothelioma and Kasabach-Merritt phenomenon who had rapid and dramatic response to sirolimus (0.1 mg/kg/day). This case provides further rationale for clinical trials of sirolimus in the treatment of vascular lesions.

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Year:  2010        PMID: 20730884     DOI: 10.1002/pbc.22766

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  22 in total

1.  Variable response to propranolol treatment of kaposiform hemangioendothelioma, tufted angioma, and Kasabach-Merritt phenomenon.

Authors:  Yvonne E Chiu; Beth A Drolet; Francine Blei; Manuel Carcao; Jason Fangusaro; Michael E Kelly; Alfons Krol; Sabra Lofgren; Anthony J Mancini; Denise W Metry; Michael Recht; Robert A Silverman; Wynnis L Tom; Elena Pope
Journal:  Pediatr Blood Cancer       Date:  2012-02-02       Impact factor: 3.167

2.  Medical therapy for pediatric vascular anomalies.

Authors:  Judith F Margolin; Heather Mills Soni; Sheena Pimpalwar
Journal:  Semin Plast Surg       Date:  2014-05       Impact factor: 2.314

Review 3.  Kaposiform hemangioendothelioma in children: a benign vascular tumor with multiple treatment options.

Authors:  Irene Schmid; Anne K Klenk; Monika Sparber-Sauer; Ewa Koscielniak; Rebecca Maxwell; Beate Häberle
Journal:  World J Pediatr       Date:  2018-07-27       Impact factor: 2.764

4.  Kasabach-Merritt phenomenon in Chinese children: Report of 19 cases and brief review of literature.

Authors:  Si-Ming Yuan; Wei-Min Shen; Hai-Ni Chen; Zhi-Jian Hong; Hui-Qing Jiang
Journal:  Int J Clin Exp Med       Date:  2015-06-15

5.  Kaposiform hemangioendothelioma without cutaneous involvement.

Authors:  Yi Ji; Siyuan Chen; Lizhi Li; Kaiying Yang; Chunchao Xia; Li Li; Gang Yang; Feiteng Kong; Guoyan Lu; Xingtao Liu
Journal:  J Cancer Res Clin Oncol       Date:  2018-10-06       Impact factor: 4.553

6.  Sirolimus for the treatment of children with various complicated vascular anomalies.

Authors:  Herwig Lackner; Anna Karastaneva; Wolfgang Schwinger; Martin Benesch; Petra Sovinz; Markus Seidel; Daniela Sperl; Sofia Lanz; Emir Haxhija; Friedrich Reiterer; Erich Sorantin; Christian E Urban
Journal:  Eur J Pediatr       Date:  2015-06-04       Impact factor: 3.183

7.  Sirolimus for treatment of kaposiform hemangioendothelioma associated with Kasabach-Merritt phenomenon.

Authors:  Alaa M Alaqeel; Nuha A Alfurayh; Alanoud A Alhedyani; Saad M Alajlan
Journal:  JAAD Case Rep       Date:  2016-12-05

8.  Exome sequence analysis of Kaposiform hemangioendothelioma: identification of putative driver mutations.

Authors:  Sho Egashira; Masatoshi Jinnin; Miho Harada; Shinichi Masuguchi; Satoshi Fukushima; Hironobu Ihn
Journal:  An Bras Dermatol       Date:  2016 Nov-Dec       Impact factor: 1.896

9.  Impact of sirolimus treatment for refractory kaposiform hemangioendothelioma with exacerbation of the disease 10 years after initial diagnosis.

Authors:  Naoki Sakata; So-Ichi Suenobu; Munehiro Okano; Satoshi Ueda; Masatomo Kimura; Tsukasa Takemura
Journal:  Rare Tumors       Date:  2018-05-30

10.  Treatment of cystic hygroma in a young infant through multidisciplinary approach involving sirolimus, sclerotherapy, and debulking surgery.

Authors:  Haya Azouz; Haneen Salah; Saad Al-Ajlan; Mohammad Badran
Journal:  JAAD Case Rep       Date:  2016-08-25
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