Literature DB >> 29233209

Rapid regression of large cardiac rhabdomyomas in neonates after sirolimus therapy.

M David Weiland1, Kristin Bonello2, Kevin D Hill1.   

Abstract

Cardiac rhabdomyomas are the most common tumours in children and are typically seen in association with the tuberous sclerosis complex. Although benign and often associated with spontaneous regression, in rare circumstances surgical resection is indicated to relieve obstruction or other mass-related effects. Recent clinical trials have demonstrated the benefits of mammalian target of rapamycin inhibitors for the treatment of other tumour sub-types associated with tuberous sclerosis. Here we report rapid regression of several massive cardiac rhadomyomas in two neonates with the use of the mammalian target of rapamycin inhibitor sirolimus.

Entities:  

Keywords:  Rhabdomyoma; sirolimus; tuberous sclerosis complex

Mesh:

Substances:

Year:  2017        PMID: 29233209     DOI: 10.1017/S104795111700244X

Source DB:  PubMed          Journal:  Cardiol Young        ISSN: 1047-9511            Impact factor:   1.093


  3 in total

1.  Congenital cardiac masses: a case report.

Authors:  Mohammed Alsabri; Alejandro Gonzalez; Aaron Sircy; Sai Sarada Policherla; Kemi Mascoll-Robertson
Journal:  J Med Case Rep       Date:  2022-04-22

Review 2.  Treatment of Cardiac Rhabdomyomas with mTOR Inhibitors in Children with Tuberous Sclerosis Complex-A Systematic Review.

Authors:  Monika Sugalska; Anna Tomik; Sergiusz Jóźwiak; Bożena Werner
Journal:  Int J Environ Res Public Health       Date:  2021-05-05       Impact factor: 3.390

3.  Sirolimus in Infants with Multiple Cardiac Rhabdomyomas Associated with Tuberous Sclerosis Complex.

Authors:  Maurizio Lucchesi; Enrico Chiappa; Flavio Giordano; Francesco Mari; Lorenzo Genitori; Iacopo Sardi
Journal:  Case Rep Oncol       Date:  2018-06-28
  3 in total

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