Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI

Purpose This study compared clinical and radiologic differences between cystic biliary atresia (cBA) and choledochal cyst (CC) type Ia/b. Methods Infants (≤12 months old) who were diagnosed with cBA or CC type Ia/b from 2005 to 2019 were retrospectively reviewed. Imaging features on preoperative ult...

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Main Authors: Hyun Joo Shin, Haesung Yoon, Seok Joo Han, Kyong Ihn, Hong Koh, Ja-Young Kwon, Mi-Jung Lee
Format: Article
Language:English
Published: Korean Society of Ultrasound in Medicine 2021-04-01
Series:Ultrasonography
Subjects:
Online Access:http://www.e-ultrasonography.org/upload/usg-20061.pdf
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spelling doaj-432626ab339d4b1299d2218680e457702021-03-23T00:51:03ZengKorean Society of Ultrasound in MedicineUltrasonography2288-59192288-59432021-04-0140230131110.14366/usg.200611133Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRIHyun Joo Shin0Haesung Yoon1Seok Joo Han2Kyong Ihn3Hong Koh4Ja-Young Kwon5Mi-Jung Lee6 Department of Radiology, Severance Hospital, Research Institute of Radiological Science, Seoul, Korea Department of Radiology, Severance Hospital, Research Institute of Radiological Science, Seoul, Korea Severance Pediatric Liver Disease Research Group, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea Severance Pediatric Liver Disease Research Group, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea Severance Pediatric Liver Disease Research Group, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea Department of Radiology, Severance Hospital, Research Institute of Radiological Science, Seoul, KoreaPurpose This study compared clinical and radiologic differences between cystic biliary atresia (cBA) and choledochal cyst (CC) type Ia/b. Methods Infants (≤12 months old) who were diagnosed with cBA or CC type Ia/b from 2005 to 2019 were retrospectively reviewed. Imaging features on preoperative ultrasonography (US) and magnetic resonance imaging (MRI) were compared between the cBA and CC groups. Logistic regression and area under the receiver operating characteristic curve (AUC) analyses were performed for the diagnosis of cBA. Changes in cyst size were also evaluated when prenatal US exams were available. Results Ten patients (5.5% of biliary atresia cases) with cBA (median age, 48 days) and 11 infants with CC type Ia/b (Ia:Ib=10:1; median age, 20 days) were included. Triangular cord thickness on US (cutoff, 4 mm) showed 100% sensitivity and 90.9% specificity (AUC, 0.964; 95% confidence interval [CI], 0.779 to 1.000) and cyst size on MRI (cutoff, 2.2 cm) had 70% sensitivity and 100% specificity (AUC, 0.900; 95% CI, 0.690 to 0.987) for diagnosing cBA. Gallbladder mucosal irregularity on US and an invisible distal common bile duct on MRI were only seen in the cBA group (10 of 10). Only the CC group showed prenatal cysts exceeding 1 cm with postnatal enlargement. Conclusion Small cyst size (<1 cm) on prenatal US, triangular cord thickening (≥4 mm) and gallbladder mucosal irregularity on postnatal US, and small cyst size (≤2.2 cm) and an invisible distal common bile duct on MRI can discriminate cBA from CC type Ia/b in infancy.http://www.e-ultrasonography.org/upload/usg-20061.pdfbiliary atresiacholedochal cystneonatal jaundiceultrasonographymagnetic resonance imaging
collection DOAJ
language English
format Article
sources DOAJ
author Hyun Joo Shin
Haesung Yoon
Seok Joo Han
Kyong Ihn
Hong Koh
Ja-Young Kwon
Mi-Jung Lee
spellingShingle Hyun Joo Shin
Haesung Yoon
Seok Joo Han
Kyong Ihn
Hong Koh
Ja-Young Kwon
Mi-Jung Lee
Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI
Ultrasonography
biliary atresia
choledochal cyst
neonatal jaundice
ultrasonography
magnetic resonance imaging
author_facet Hyun Joo Shin
Haesung Yoon
Seok Joo Han
Kyong Ihn
Hong Koh
Ja-Young Kwon
Mi-Jung Lee
author_sort Hyun Joo Shin
title Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI
title_short Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI
title_full Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI
title_fullStr Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI
title_full_unstemmed Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI
title_sort key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and mri
publisher Korean Society of Ultrasound in Medicine
series Ultrasonography
issn 2288-5919
2288-5943
publishDate 2021-04-01
description Purpose This study compared clinical and radiologic differences between cystic biliary atresia (cBA) and choledochal cyst (CC) type Ia/b. Methods Infants (≤12 months old) who were diagnosed with cBA or CC type Ia/b from 2005 to 2019 were retrospectively reviewed. Imaging features on preoperative ultrasonography (US) and magnetic resonance imaging (MRI) were compared between the cBA and CC groups. Logistic regression and area under the receiver operating characteristic curve (AUC) analyses were performed for the diagnosis of cBA. Changes in cyst size were also evaluated when prenatal US exams were available. Results Ten patients (5.5% of biliary atresia cases) with cBA (median age, 48 days) and 11 infants with CC type Ia/b (Ia:Ib=10:1; median age, 20 days) were included. Triangular cord thickness on US (cutoff, 4 mm) showed 100% sensitivity and 90.9% specificity (AUC, 0.964; 95% confidence interval [CI], 0.779 to 1.000) and cyst size on MRI (cutoff, 2.2 cm) had 70% sensitivity and 100% specificity (AUC, 0.900; 95% CI, 0.690 to 0.987) for diagnosing cBA. Gallbladder mucosal irregularity on US and an invisible distal common bile duct on MRI were only seen in the cBA group (10 of 10). Only the CC group showed prenatal cysts exceeding 1 cm with postnatal enlargement. Conclusion Small cyst size (<1 cm) on prenatal US, triangular cord thickening (≥4 mm) and gallbladder mucosal irregularity on postnatal US, and small cyst size (≤2.2 cm) and an invisible distal common bile duct on MRI can discriminate cBA from CC type Ia/b in infancy.
topic biliary atresia
choledochal cyst
neonatal jaundice
ultrasonography
magnetic resonance imaging
url http://www.e-ultrasonography.org/upload/usg-20061.pdf
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