Computed tomography and magnetic resonance imaging of multiple focal nodular hyperplasias of the liver with congenital absence of the portal vein in a Chinese girl: case report and review of the literature.

Abstract:

BACKGROUND:Patients with congenital absence of the portal vein (CAPV) often suffer from additional medical complications such as hepatic tumors and cardiac malformations. CASE PRESENTATION:Congenital absence of the portal vein (CAPV) is a rare malformation. We present a case of a 16-year-old Chinese girl with CAPV with multiple pathology-proven hepatic focal nodular hyperplasias (FNHs) and ventricular septal defect (VSD). The CT and MRI features of this case are described, and previously reported cases are reviewed. CONCLUSIONS:CAPV is a rare congenital anomaly and in such patients, clarifying the site of portosystemic shunts, liver disease, and other anomalies is critical for appropriate treatment selection and accurate prognosis determination. Close follow-up, including laboratory testing and radiologic imaging, is recommended for all CAPV patients.

journal_name

Eur J Med Res

authors

Zhang K,Wang Q,Wang H,Ye H,Guo A,Duan W

doi

10.1186/s40001-014-0063-7

subject

Has Abstract

pub_date

2014-11-26 00:00:00

pages

63

eissn

0949-2321

issn

2047-783X

pii

s40001-014-0063-7

journal_volume

19

pub_type

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