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A RARE TUMOR OF THE LUNG IN CHILDHOOD – INFLAMMATORY MYOFIBROBLASTIC TUMOR

Mirko Žganjer
Igor Nikolić
Ante Čizmić
Marko Mesić
Božidar Župančić

Puni tekst: hrvatski, pdf (234 KB) str. 0-0 preuzimanja: 154* citiraj
APA 6th Edition
Žganjer, M., Nikolić, I., Čizmić, A., Mesić, M. i Župančić, B. (2014). RIJETKI TUMOR PLUĆA U DJEČJOJ DOBI – INFLAMATORNI MIOFIBROBLASTIČNI TUMOR. Liječnički vjesnik, 136 (1-2), 0-0. Preuzeto s https://hrcak.srce.hr/172582
MLA 8th Edition
Žganjer, Mirko, et al. "RIJETKI TUMOR PLUĆA U DJEČJOJ DOBI – INFLAMATORNI MIOFIBROBLASTIČNI TUMOR." Liječnički vjesnik, vol. 136, br. 1-2, 2014, str. 0-0. https://hrcak.srce.hr/172582. Citirano 24.10.2019.
Chicago 17th Edition
Žganjer, Mirko, Igor Nikolić, Ante Čizmić, Marko Mesić i Božidar Župančić. "RIJETKI TUMOR PLUĆA U DJEČJOJ DOBI – INFLAMATORNI MIOFIBROBLASTIČNI TUMOR." Liječnički vjesnik 136, br. 1-2 (2014): 0-0. https://hrcak.srce.hr/172582
Harvard
Žganjer, M., et al. (2014). 'RIJETKI TUMOR PLUĆA U DJEČJOJ DOBI – INFLAMATORNI MIOFIBROBLASTIČNI TUMOR', Liječnički vjesnik, 136(1-2), str. 0-0. Preuzeto s: https://hrcak.srce.hr/172582 (Datum pristupa: 24.10.2019.)
Vancouver
Žganjer M, Nikolić I, Čizmić A, Mesić M, Župančić B. RIJETKI TUMOR PLUĆA U DJEČJOJ DOBI – INFLAMATORNI MIOFIBROBLASTIČNI TUMOR. Liječnički vjesnik [Internet]. 2014 [pristupljeno 24.10.2019.];136(1-2):0-0. Dostupno na: https://hrcak.srce.hr/172582
IEEE
M. Žganjer, I. Nikolić, A. Čizmić, M. Mesić i B. Župančić, "RIJETKI TUMOR PLUĆA U DJEČJOJ DOBI – INFLAMATORNI MIOFIBROBLASTIČNI TUMOR", Liječnički vjesnik, vol.136, br. 1-2, str. 0-0, 2014. [Online]. Dostupno na: https://hrcak.srce.hr/172582. [Citirano: 24.10.2019.]

Sažetak
Inflammatory myofibroblastic tumor (IMT) is a rare benign neoplasm, mainly involving the lungs of the children. It represents 0.7% of all lung tumors.1 It was first described by Brunn in 1939.2 Diagnosis is very difficult and often only possible after resection of the tumor. We would like to present a case of pulmonary IMT in a 13-year-old girl who presented with symptoms like cough, shortness of breath , and chest discomfort. Chest X ray and computed tomography revealed the presence of a right lower lobe lung mass. Its clinical and radiological findings were diverse and non specific. The mass was removed in toto, histopathology confirmed the inflammatory myofibroblastic tumor of the lung. Intraoperative and postoperative courses were uneventful. The patient has been without any signs of relapse 2 years after the surgery.

Ključne riječi
Lung neoplasms – diagnosis, pathology, surgery; Neoplasms, muscle tissue – diagnosis, pathology, surgery; Rare diseases – diagnosis, pathology, surgery

Hrčak ID: 172582

URI
https://hrcak.srce.hr/172582

[hrvatski]

Posjeta: 287 *