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Hepatobiliary Rhabdomyosarcoma Mimicking Choledochal Cyst: Lessons Learned

Overview
Specialty General Surgery
Date 2014 Mar 19
PMID 24636980
Citations 3
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Abstract

Introduction: The differential diagnosis of hepatic cystic lesions is a challenging process especially in case of hepatic rhabdomyosarcoma (HRMS) presenting as hepatic cyst.

Presentation Of Case: We introduce our experience with a case of HRMS in a 3-year-old female patient who was misdiagnosed to have type IV-A choledochal cyst and definitive correct diagnosis was reached after the pathological and immunohistochemical examination of the surgically resected lesion. This case presentation is followed by important practical messages to hepatobiliary surgeons regarding HRMS.

Discussion: HRMS is a rare pediatric tumor. Jaundice is the most common presentation of HRMS followed by abdominal pain and vomiting. Great effort is needed to differentiate the tumor from choledochal cyst and infectious hepatitis. Through evaluation using available imaging studies together with clinical anticipation is mandatory for establishing the correct diagnosis.

Conclusion: Differentiation of HRMs from choledochal cyst mandates through evaluation and clinical anticipation. HRMS should be suspected in any child with obstructive jaundice. Once diagnosis is established, multidisciplinary treatment is the best management strategy and it has proved better surgical outcome and long term survival.

Citing Articles

Rhabdomyosarcoma of the Biliary Tract in Children: Analysis of Single Center Experience.

Swieszkowska E, Broniszczak D, Kalicinski P, Szymczak M, Stefanowicz M, Grajkowska W Cancers (Basel). 2024; 16(17).

PMID: 39272968 PMC: 11394218. DOI: 10.3390/cancers16173110.


Pencil Beam Scanning Proton Therapy for Rhabdomyosarcoma of the Biliary Tract.

Pater L, Turpin B, Mascia A Cureus. 2017; 9(10):e1747.

PMID: 29226038 PMC: 5716683. DOI: 10.7759/cureus.1747.


Pediatric choledochal cysts: diagnosis and current management.

Soares K, Goldstein S, Ghaseb M, Kamel I, Hackam D, Pawlik T Pediatr Surg Int. 2017; 33(6):637-650.

PMID: 28364277 DOI: 10.1007/s00383-017-4083-6.

References
1.
RUYMANN F, Raney Jr R, Crist W, LAWRENCE Jr W, Lindberg R, Soule E . Rhabdomyosarcoma of the biliary tree in childhood. A report from the Intergroup Rhabdomyosarcoma Study. Cancer. 1985; 56(3):575-81. DOI: 10.1002/1097-0142(19850801)56:3<575::aid-cncr2820560326>3.0.co;2-9. View

2.
Davis G, KISSANE J, Ishak K . Embryonal rhabdomyosarcoma (sarcoma botryoides) of the biliary tree. Report of five cases and a review of the literature. Cancer. 1969; 24(2):333-42. DOI: 10.1002/1097-0142(196908)24:2<333::aid-cncr2820240216>3.0.co;2-g. View

3.
Zampieri N, Camoglio F, Corroppolo M, Cecchetto M, Ornis S, Ottolenghi A . Botryoid rhabdomyosarcoma of the biliary tract in children: a unique case report. Eur J Cancer Care (Engl). 2006; 15(5):463-6. DOI: 10.1111/j.1365-2354.2006.00683.x. View

4.
Sanz , de Mingo L , Florez , Rollan V . Rhabdomyosarcoma of the biliary tree. Pediatr Surg Int. 1997; 12(2/3):200-1. View

5.
Kumar V, Chaudhary S, Kumar M, Gangopadhyay A . Rhabdomyosarcoma of biliary tract- a diagnostic dilemma. Indian J Surg Oncol. 2013; 3(4):314-6. PMC: 3521542. DOI: 10.1007/s13193-012-0186-7. View