| Literature DB >> 24814936 |
Hisanori Fujino1, Young-Dong Park, Suguru Uemura, Shinzo Tanaka, Masakazu Kawabe, Sayaka Maeda, Itaru Kato, Ken-Ichiro Watanabe, Katsutsugu Umeda, Hidefumi Hiramatsu, Souichi Adachi, Toshihiko Sato, Hiroshi Date, Hironori Haga, Shinichi Sumimoto.
Abstract
IMTs belong to the group of soft tissue tumor and could occur at any anatomical site; however, the causes and growth feature remain unclear. This case report documents a 10-yr-old male suffering from slowly developing dyspnea on exertion and cough around seven months post-HCT. He was diagnosed with an endobronchial tumor based on imaging, and histology confirmed ALK-positive submucosal spindle-shaped cells with infiltrative cells, compatible with IMT. We should be aware that IMT is a potential complication of pediatric allogeneic HCT and can cause sudden airway obstruction.Entities:
Keywords: bone marrow transplantation; lung diseases
Mesh:
Year: 2014 PMID: 24814936 DOI: 10.1111/petr.12275
Source DB: PubMed Journal: Pediatr Transplant ISSN: 1397-3142