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Amirikar, Farinaz, Bilan, Nemat, Rezamand, Azim, Jamshidi, Masoud, Golchinfar, Zahra. (1401). Rhabdomyosarcoma Arising within Congenital Cystic Adenomatoid Malformation; a Case Report. , 10(6), 16233-16237. doi: 10.22038/ijp.2022.64392.4889
Farinaz Amirikar; Nemat Bilan; Azim Rezamand; Masoud Jamshidi; Zahra Golchinfar. "Rhabdomyosarcoma Arising within Congenital Cystic Adenomatoid Malformation; a Case Report". , 10, 6, 1401, 16233-16237. doi: 10.22038/ijp.2022.64392.4889
Amirikar, Farinaz, Bilan, Nemat, Rezamand, Azim, Jamshidi, Masoud, Golchinfar, Zahra. (1401). 'Rhabdomyosarcoma Arising within Congenital Cystic Adenomatoid Malformation; a Case Report', , 10(6), pp. 16233-16237. doi: 10.22038/ijp.2022.64392.4889
Amirikar, Farinaz, Bilan, Nemat, Rezamand, Azim, Jamshidi, Masoud, Golchinfar, Zahra. Rhabdomyosarcoma Arising within Congenital Cystic Adenomatoid Malformation; a Case Report. , 1401; 10(6): 16233-16237. doi: 10.22038/ijp.2022.64392.4889

Rhabdomyosarcoma Arising within Congenital Cystic Adenomatoid Malformation; a Case Report

Journal of Pediatric Perspectives
مقاله 14، دوره 10، شماره 6، شهریور 2022، صفحه 16233-16237    اصل مقاله (505.71 K)
نوع مقاله: case report
شناسه دیجیتال (DOI): 10.22038/ijp.2022.64392.4889
نویسندگان
Farinaz Amirikar* 1؛ Nemat Bilan1؛ Azim Rezamand2؛ Masoud Jamshidi1؛ Zahra Golchinfar3
1Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, IR Iran
3Clinical Research Development Unit of Children Educational and Treatment Center, Tabriz University of Medical Sciences, Tabriz, Iran
چکیده
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.
کلیدواژه‌ها
Rhabdomyosarcoma؛ Cystic Adenomatoid؛ Childhood
مراجع
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