Choledochal Cysts Diagnosis and Treatments: Case Report

dc.contributor.authorAl-Ba'adani, Mohamed Noaman
dc.contributor.authorAlammari, Saleh Ahmed
dc.contributor.authorJumman, Najwa Aziz
dc.date.accessioned2026-10-23T21:14:36Z
dc.date.issued2022
dc.description.abstractCholedochal cyst is a rare pathological condition, which represents 1% of benign diseases of the biliary tract. It is seen with significant frequency in childhood, with a higher prevalence in females. Diagnosis is primarily based on clinical suspicion. Its symptoms are variable and its treatment, depending on the type, is surgical. Case Report: A 5-year-old female childhood, weighing 20 kg presented with a two weeks history of upper abdominal pain, jaundice and low-grade fever for 8 days, accompanied by high colored urine, and pale colored stools. Our case diagnosis was made by biochemical parameters and ultrasonography, CT-scan. The recurrent cholangitis, pancreatitis and malignant diseases associated with choledochal cysts mandate early diagnosis and definitive surgical management.
dc.identifier.citationAl-Ba'adani, M. N., Alammari, S. A., & Jumman, N. A. (2022). Choledochal cysts diagnosis and treatments: Case report. Open Access Library Journal, 9(2), Article e7382. https://doi.org/10.4236/oalib.1107382
dc.identifier.doi10.4236/oalib.1107382
dc.identifier.issn2333-9721
dc.identifier.issn2333-9705
dc.identifier.urihttps://doi.org/10.4236/oalib.1107382
dc.identifier.urihttps://www.oalib.com/paper/6528309
dc.identifier.urihttps://repository.ust.edu.ye/handle/123456789/3011
dc.language.isoen
dc.publisherScientific Research Publishing, Inc.
dc.relation.ispartofOpen Access Library Journal
dc.subjectCholedochal Cyst
dc.subjectBile Duct Cyst
dc.titleCholedochal Cysts Diagnosis and Treatments: Case Report
dc.typeArticle

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