Rhabdomyosarcoma Arising within Congenital Cystic Adenomatoid Malformation; a Case Report
نویسندگان
1 Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2 Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
3 Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, IR Iran
4 Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
5 Clinical Research Development Unit of Children Educational and Treatment Center, Tabriz University of Medical Sciences, Tabriz, Iran
doi
10.22038/ijp.2022.64392.4889چکیده
This case report describes a 30-month-old child with primary pulmonary rhabdomyosarcoma with a congenital cystic adenomatoid malformation (CCAM). In the current literature, primary pulmonary neoplasms have been reported for similar cases. The tumor was located in the anterior-basal segment of the left lower lobe with a thin-walled cystic appearance and lobulated margins. A histology examination showed rhabdomyosarcoma origin with an embryonal subtype. Postoperative systemic chemotherapy was carried out. After a 6-month follow-up, the patient had no residual or recurrent disease.
