一例 IV 型胆总管囊肿病例

Q4 Medicine

Radiology Case Reports Pub Date : 2024-11-07 DOI:10.1016/j.radcr.2024.10.033

Dian Komala Dewi , Oki Kurniawan , Dudus Indra Gunawan , Harry Galuh Nugraha

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A case of choledochal cyst type IV

A choledochal cyst (CC) or biliary cyst is a congenital or acquired anomaly affecting the biliary tree. It involves the dilation of the biliary tree that could affect the extrahepatic and/or the intrahepatic segments. A choledochal cyst (CC) has traditionally been considered as a cystic dilation of the extrahepatic bile duct. The incidence of choledochal cysts is high in the Asian population with a female predominance. Choledochal cysts can present at any age, including infancy. However, 80% of choledochal cysts are diagnosed in the first decade of life, with cholestasis being the most common sign in infants, and cholangitis or pancreatitis being less common. Radiological and endoscopic imaging is the cornerstone of CC diagnosis. We report a case of 16 years old patient with choledocal cyst. The case has distinct clinical signs that are easily recognizable.

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来源期刊

Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging

CiteScore

1.10

自引率

0.00%

发文量

1074

审稿时长

30 days

期刊介绍： The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.