| Literature DB >> 33328007 |
Hassan Nazmul1, Islam Rafiqul1, Fathema Kaniz1, Sayeed Maimuna1, Wahiduzzaman Mazumder Md1, Bazlul Karim Asm1, Pada Dey Bishnu2.
Abstract
Extrahepatic biliary tract tumors are rare and among them rhabdomyosarcoma is most common. Rhabdomyosarcoma is a soft tissue malignant musculoskeletal tumor and is a very rare malignancy of the common bile duct in children. It usually presents as obstructive jaundice and/or pruritus. If there is no local invasion to the adjacent tissues, the radiological appearance of the tumor lesion is like a choledochal cyst. So the diagnosis is usually made at surgery or by preoperative biopsy. It is important to diagnose early and differentiate it from choledochal cyst and start treatment as early as possible for long time survival of the patient. This case report presented a case of a 10-year-old boy with recurrent onset of obstructive jaundice and fever preoperatively who was diagnosed as choledochal cyst and postoperatively as embryonal rhabdomyosarcoma of the common bile duct. After surgical resection and postoperative chemotherapy, the child had a good prognosis. So it is crucial to know that this rare tumor can mimic congenital choledochal cyst and it should be considered in the differential diagnosis of obstructive jaundice in children.Entities:
Mesh:
Year: 2020 PMID: 33328007 PMCID: PMC7735933
Source DB: PubMed Journal: Zhongguo Dang Dai Er Ke Za Zhi ISSN: 1008-8830