Embryonal rhabdomyosarcoma (sarcoma botryoides) of biliary tree in childhood: report of 1 case and literature review
- VernacularTitle:小儿胆道葡萄状肉瘤(附1例及文献复习)
- Author:
Bin LIU
- Publication Type:Journal Article
- Keywords:
Embryonal rhabdomyosarcoma;
Sarcoma botryoides;
Biliary tree;
Child
- From:
Journal of Chongqing Medical University
2003;0(06):-
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To improve the understanding and diagnosis of embryonal rhabdomysarcoma of biliary tree in childhood.Methods:The management of 1 child with sarcoma botryoides of biliary tree and other 15 cases reported were reviewed.Results:11 cases of boys and 5 of girls,varying from 1 to 6 years old.Clinical symptoms at presentation included jaundice in 16/16,fever 8/16,abdominal pain 6/16,white feces 9/16 and hepatomegaly 13/16, etc.5 cases of which were misdiagnosed as having hepatitis.There were only 2 cases considered as rhabdomyosarcoma by ultrasound and 1 by abdominal CT scan.7 cases had not recurred in 8 months after combined treatment of complete surgical excision,chemotherapy and radiotherapy.Treated with combination of partial excision and chemotherapy,1 case's tumor turned smaller 3 months later.But 2 cases treated solely with partial excision died 2 months later and 1 case recurred 2 months later.Conclusion:All rhabdomyosarcoma of biliary tree in childhood are botryoid,embryonal rhabdomyosarcoma.The patients are aged from 1 to 6 years old,and boys are more common than girls.The main clinical symptoms are obstructive jaundice,fever and hepatomegaly,so it is easily misdiagnosed as hepatitis in clinic.Ultrasound and abdominal CT sacn are helpful in diagnosing embryonal rhabdomysarcoma (sarcoma botryoides) of biliary tree,but pathological examination is essential for confirming the disease.A combined approach of aggressive surgery,chemotherapy and radiotherapy may result in long-term survival.
