Infantile Fibrosarcoma in Neonate.
10.4174/jkss.2010.79.Suppl1.S62
- Author:
So Hyun NAM
;
Min Jung CHO
;
Dae Yeon KIM
;
Seong Chul KIM
;
In Koo KIM
- Publication Type:Case Report
- Keywords:
Infantile fibrosarcoma;
Congenital lymphangioma;
Congenital hemangioma;
Congenital bowel obstruction
- MeSH:
Chemotherapy, Adjuvant;
Child;
Colon, Transverse;
Fibrosarcoma;
Hemangioma;
Humans;
Infant, Newborn;
Lymphangioma;
Magnetic Resonance Spectroscopy;
Parturition;
Picibanil;
Recurrence;
Thigh
- From:Journal of the Korean Surgical Society
2010;79(Suppl 1):S62-S66
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Infantile fibrosarcoma is a rare malignant soft tissue tumor occurring especially in newborn and young children under 2 years. We experienced three cases of infantile fibrosarcoma presenting in the neonatal period. Case 1 presented with a multiseptated cystic mass on his left thigh at birth that was diagnosed as lymphangioma. After picibanil injection, we noted the size of the mass doubled and a solid lesion was prominent in the magnetic resonance image. Case 2 was found to have a reddish mass on his lower back mimicking hemangioma. Over 2 weeks, the mass grew rapidly with internal hemorrhaging. Case 3 was noted to have an encircling mass around the splenic flexure, which developed into congenital bowel obstruction. All of the tumors were resected completely, but microscopic resection margin was not clear in two patients. The two patients received adjuvant chemotherapy and all patients are well without evidence of recurrence.
