Abstract
Abstract
Background
Biliary hamartomas are rare benign bile duct malformations consisting of multiple collections of localized duct-like structures that are lined by biliary epithelium and embedded in a fibrous stroma. In general, these malformations are asymptomatic and are usually detected incidentally during imaging, surgical exploration, or autopsy. Previously, the definitive diagnosis of these lesions was possible only with liver biopsy. The use of advanced imaging modalities made it possible to establish the diagnosis when undoubtful imaging findings are evident.
Case presentation
We present a 25-day-old male newborn who was referred to our institution with jaundice, abdominal distension, and abdominal U/S that revealed hepatomegaly and involvement of both lobes of the liver with diffuse cystic lesions of variable sizes and echogenicity without a diagnostic suggestion. We discuss the details of imaging findings that enabled to establish the diagnosis of multiple biliary hamartomas and brief the patient’s status on follow-up.
Conclusion
Up to our best knowledge, the diagnosis of multiple biliary hamartomas has not been previously reported among newborns, making this report an extremely rare if not a unique observation.
Publisher
Springer Science and Business Media LLC
Reference11 articles.
1. Teng SL, Shin JS, Huang JC (2015) An unusual polynodular liver disease: multiple biliary hamartoma. Advances in Digestive Medicine 2(1):37–40
2. Singh Y, Cawich SO, Ramjit C, Naraynsingh V (2016) Rare liver tumor: symptomatic giant von Meyenburg complex. Journal of Surgical Case Reports 11:1–4
3. Markhardt BK, Rubens DJ, Huang J, Dogra VS (2006) Sonographic features of biliary hamartomas with histopathologic correlation. J Ultrasound Med 25:1631–1633
4. Zheng RQ, Zhang B, Kudo M, Onda H, Inoue T (2005) Imaging findings of biliary hamartomas. World J Gastroenterol 11:6354–6359
5. Jáquez-Quintana JO, Reyes-Cabello EA, Bosques-Padilla FJ (2017) Multiple biliary hamartomas, the “von Meyenburg complexes”. Ann Hepatol 16(5):812–813