类似胆总管囊肿的胆总管横纹肌肉瘤：阻塞性黄疸的罕见原因

doi:10.7499/j.issn.1008-8830.2007118

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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.

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	Articles by authors
	Nazmul Hassan
	Rafiqul Islam
	Kaniz Fathema
	Maimuna Sayeed
	Md. Wahiduzzaman Mazumder
	ASM Bazlul Karim
	Bishnu Pada Dey

Key words： Biliary rhabdomyosarcoma Obstructive jaundice Choledochal cyst Common bile duct Child

Received: 15 July 2020

Cite this article:

Nazmul Hassan,Rafiqul Islam,Kaniz Fathema et al. Rhabdomyosarcoma of the common bile duct mimicking choledochal cyst: a rare cause of obstructive jaundice[J]. CJCP, 2020, 22(12): 1338-1343.

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http://www.zgddek.com/EN/10.7499/j.issn.1008-8830.2007118 OR http://www.zgddek.com/EN/Y2020/V22/I12/1338

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