Two Cases of Infantile Intra-abdominal Inflammatory Myofibroblastic Tumor
1
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
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.
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.
참고문헌 (12)
- Eun Young Kim, "Inflammatory myofibroblastic tumor in colon", 대한외과학회지, 82(1), pp.45~49 (2012), 대한외과학회
- Kovach SJ, "Inflammatory myofibroblastic tumors", J Surg Oncol, 94, pp.385~391 (2006)
- Kim HY, "Abdominal inflammatory myofibroblastic tumor in children", J Korean Assoc Pediatr Surg, 14, pp.153~163 (2008)
- Kim SJ, "Inflammatory myofibroblastic tumors of the abdomen as mimickers of malignancy: imaging features in nine children", AJR Am J Roentgenol, 193, pp.1419~1424 (2009)
- Singhal M, "Omental inflammatory myofibroblastic tumour mimicking peritoneal carcinomatosis", Cancer Imaging, 11, pp.19~22 (2011)
- Ong HS, "Head and neck inflammatory myofibroblastic tumor (IMT): evaluation of clinicopathologic and prognostic features", Oral Oncol, 48, pp.141~148 (2012)
- Fragoso AC, "Abdominal inflammatory myofibroblastic tumor a clinicopathologic study with reappraisal of biologic behavior", J Pediatr Surg, 46, pp.2076~2082 (2011)
- Woo MJ, "Inflammatory myofibroblastic tumor in a 3 months old infant", Clin Pediatr Hematol Oncol, 18, pp.62~65 (2011)
- 계봉현, "A case of inflammatory myofibroblastic tumor originated from the greater omentum in young adult", 대한외과학회지, 82(6), pp.380~384 (2012), 대한외과학회[DOI]
- Bertocchini A, "Unresectable multifocal omental and peritoneal inflammatory myofibroblastic tumor in a child: revisiting the role of adjuvant therapy", J Pediatr Surg, 46, pp.e17~e21 (2011)
- Li J, "Inflammatory myofibroblastic tumor with RANBP2 and ALK gene rearrangement: a report of two cases and literature review", Diagn Pathol, 8, pp.147~ (2013)
- Chun YS, "Pediatric inflammatory myofibroblastic tumor:anaplastic lymphoma kinase (ALK) expression and prognosis", Pediatr Blood Cancer, 45, pp.796~801 (2005)
