Start New EnglishEspañol中文РусскийالعربيةTiếng ViệtFrançaisDeutsch한국어Tagalog Library Performance
BETA v.3.0

2025 ICD-10-CM code Q44.4

Choledochal cyst

Medical necessity for treatment of a choledochal cyst is based on the potential for complications such as cholangitis, pancreatitis, and malignant transformation. The size and type of the cyst, as well as the patient's symptoms, influence treatment decisions.

Diagnosis and management of this condition are typically handled by pediatric surgeons, gastroenterologists, and hepatologists.

In simple words: A choledochal cyst is a birth defect where the bile duct, which carries bile from the liver to the gallbladder and small intestine, is abnormally widened.

A choledochal cyst is a congenital dilation of the common bile duct.

Example 1: A newborn infant presents with jaundice and abdominal distension. Imaging reveals a cystic dilation of the common bile duct, consistent with a choledochal cyst., A 2-year-old child experiences recurrent episodes of abdominal pain, fever, and jaundice.A choledochal cyst is diagnosed via ultrasound., An adult undergoes an abdominal ultrasound for unrelated reasons, and a choledochal cyst is incidentally discovered.

Documentation should include imaging findings (e.g., ultrasound, CT, MRI) confirming the presence of a choledochal cyst, as well as any associated symptoms or complications.

** Choledochal cysts are classified into several types based on their location and morphology.Treatment typically involves surgical excision of the cyst.

** Only Enterprise users with EHR integration can access case-specific answers. Click here to request access.

Discover what matters.

iFrame™ AI's knowledge is aligned with and limited to the materials uploaded by users and should not be interpreted as medical, legal, or any other form of advice by iFrame™.