@article{JTD25550,
author = {Wei Wang and Ying-Ying Gu and Yu-Hong Dong and Ji-Gang Wang and Dong-Liang Lin and Cong-Juan Luo and Li Zhang and Xiao-Bin Ji and Yan Wang},
title = {Rhabdomyoma of the pleura: a case report},
journal = {Journal of Thoracic Disease},
volume = {10},
number = {12},
year = {2018},
keywords = {},
abstract = {Rhabdomyoma is a rare benign soft tissue tumor deriving from striated muscle. It can be classified generally into two subtypes according to the location: cardiac rhabdomyoma and extracardiac rhabdomyoma. Cardiac rhabdomyoma manifests as well-defined solitary or multifocal nodules in heart consisting myocardial-like tumor cells with rich cytoplasm, which is more common in kids and associated with tuberous sclerosis (1). Extracardiac rhabdomyoma can be divided into three groups according to morphological features (adult, fetal, and genital types). The adult and fetal types mainly occur in the head and neck region, while the genital type usually occurs in the genital tract.},
issn = {2077-6624}, url = {https://jtd.amegroups.org/article/view/25550}
}