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BMJ Case Rep ; 20182018 Jun 13.
Article in English | MEDLINE | ID: mdl-29898912

ABSTRACT

Biliary cystic disease is a rare entity. Twenty-five per cent of cases are diagnosed during adulthood and only a few reports have described this condition during pregnancy, where it represents a therapeutic challenge for both obstetricians and surgeons with regard to the risks it entails for the patient and the fetus.Definitive management is surgical resection, as cysts may progress to malignancy if untreated. During pregnancy, resection is generally deferred to after delivery, especially in the context of suspected cholangitis.A 19-year-old young woman with no previous prenatal control, presented to the emergency department on her 32nd week of gestation with abdominal pain and jaundice. A giant Todani I biliary cyst was observed on imaging along with dilation of the proximal biliary tree suggesting acute cholangitis. Fetal compromise prompted immediate delivery after which percutaneous biliary drainage was performed. Following recovery, the cyst was surgically resected.


Subject(s)
Choledochal Cyst/diagnostic imaging , Choledochal Cyst/surgery , Drainage/instrumentation , Pregnancy Trimester, Third , Abdominal Pain/diagnosis , Abdominal Pain/etiology , Cholangiopancreatography, Magnetic Resonance/methods , Choledochal Cyst/pathology , Delivery, Obstetric/standards , Diagnosis, Differential , Drainage/methods , Female , Humans , Jaundice/diagnosis , Jaundice/etiology , Pregnancy , Rare Diseases , Treatment Outcome , Young Adult
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