Hershey Marcus, James Casie M, Velez Maria, Kanotra Jhanvi, Craver Randall, Kanotra Sohit Paul
Department of Otolaryngology-Head and Neck Surgery, Louisiana State University, Louisiana, USA.
Section of Hematology and Oncology, Children's Hospital New Orleans, Louisiana State University, Louisiana, USA.
J Indian Assoc Pediatr Surg. 2019 Jul-Sep;24(3):212-215. doi: 10.4103/jiaps.JIAPS_107_18.
We describe a posterior wall intratracheal embryonal rhabdomyosarcoma (RMS) arising in a 6-year-old tracheostomized child masquerading as reactive granulation tissue and review all reported cases of pediatric intratracheal RMS. The child underwent laser debulking of the tumor and postoperative radiation and chemotherapy with no evidence of recurrence at 2-year follow-up. A literature review revealed four previous cases of pediatric primary tracheal or intratracheal RMS, and remission was achieved in all but one case with surgery, chemotherapy, and radiation. Pathologic evaluation of tracheal mucosal granulation tissue may merit consideration, particularly in patients with increased risk factors.
我们描述了一例发生在一名6岁气管切开患儿的气管后壁气管内胚胎性横纹肌肉瘤(RMS),该肿瘤伪装成反应性肉芽组织,并回顾了所有报道的小儿气管内RMS病例。该患儿接受了肿瘤激光减容术及术后放疗和化疗,在2年随访中无复发迹象。文献综述显示,此前有4例小儿原发性气管或气管内RMS病例,除1例患者外,其余所有病例通过手术、化疗和放疗均实现缓解。气管黏膜肉芽组织的病理评估值得考虑,尤其是在具有增加风险因素的患者中。