Complete resection of a huge hypervascular inflammatory myofibroblastic tumor in right hemithorax after embolization
- Authors
- Kim, Kyu-Nam; Kim, Dong-Won
- Issue Date
- Nov-2016
- Publisher
- Springer Verlag
- Keywords
- embolization; granuloma; mediastinal neoplasms; plasma cell
- Citation
- World Journal of Pediatrics, v.12, no.4, pp 498 - 500
- Pages
- 3
- Indexed
- SCIE
SCOPUS
- Journal Title
- World Journal of Pediatrics
- Volume
- 12
- Number
- 4
- Start Page
- 498
- End Page
- 500
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153629
- DOI
- 10.1007/s12519-016-0038-6
- ISSN
- 1708-8569
1867-0687
- Abstract
- Background
Inflammatory myofibroblastic tumor (IMT) is a rare and mostly benign tumor that has the possibility of malignant change.
Methods
Radiological findings revealed a huge mass that filled most of the right hemithorax of a 17-monthold female infant. Tumor extirpation was stopped due to massive bleeding and limited exposure of the tumor. Embolization was conducted to obstruct the arteries feeding the mass. Complete resection was performed.
Results
Histopathologic examination led to the diagnosis of IMT. Postoperative recovery was uneventful.
Conclusion
Hypervascularity of IMT should be considered. Preoperative embolization can be effective to reduce intraoperative blood loss and facilitate the surgical procedure.
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