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KMID : 0816120140170020116
Korean Journal of Pediatric Gastroenterolology and Nutrition
2014 Volume.17 No. 2 p.116 ~ p.120
Two Cases of Infantile Intra-abdominal Inflammatory Myofibroblastic Tumor
Kim Soo-Hong

Cho Yong-Hoon
Kim Hae-Young
Abstract
Inflammatory myofibroblastic tumor (IMT) is rare mesenchymal solid tumor that consists of proliferating myofibro-blasts with an inflammatory infiltrate background. It has a very low prevalence in infants and occurs mainly in children and young adults. IMT are mainly located in the thoracic cavity, but intra-abdominal lesions are rare. IMT can exhibit locally aggressive neoplastic processes and metastases similar to malignancies, so, have clinical importance. Herein, we describe two infantile intra-abdominal IMT cases presenting with incidentally found palpable abdominal mass. A 4-month-old male infant had IMT at the ileal mesentery and a 5-month-old male infant had IMT at liver. Both cases were successfully treated by complete surgical resection without complication or recurrence. Considering the biological behavior of the intermediate type of neoplasm in IMT, we expect good survivals when achieving appro-priate surgical resection without adjuvant therapy in infantile intra-abdominal IMT.
KEYWORD
Inflammatory myofibroblastic tumor, Intraabdominal, Infant
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