An Unusual Presentation of Type II Abernethy Malformation

2014 ◽  
Vol 28 (6) ◽  
pp. 1567.e1-1567.e4 ◽  
Author(s):  
Jingbo Lu ◽  
Zhiqi Lin ◽  
Hao Liu ◽  
Zhengjun Liu
2020 ◽  
Vol 65 ◽  
pp. 285.e1-285.e5
Author(s):  
Mantian Zhou ◽  
Juqiang Zhang ◽  
Lei Luo ◽  
Botian Wang ◽  
Renjun Zheng ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Zhen Kang ◽  
Xiangde Min ◽  
Liang Wang

Background. Abernethy malformation is a rare splanchnic vascular abnormality characterizing extrahepatic abnormal shunts that is classified into types I and II. Abernethy malformation type I has a female predilection and is associated with a variety of concurrent hepatic benign or malignant tumours while type II with concurrent tumours is very rare in females. Case Report. We report a rare female case of Abernethy malformation type II with concurrent occupying lesion in the right liver, which was successfully transplanted; the occupying lesion was pathologically proven to be nodular hyperplasia. Conclusion. This case might provide further knowledge regarding Abernethy malformation. On imaging, the anatomy of portal vein should be carefully investigated to categorize Abernethy malformation, and a wide variety of differential diagnosis of concurrent occupying lesions should be taken into account.


2006 ◽  
Vol 12 (1) ◽  
Author(s):  
S Chauhan ◽  
S D'Cruz ◽  
H Mohan ◽  
R Singh ◽  
J Ram ◽  
...  
Keyword(s):  

2018 ◽  
Vol 17 (5) ◽  
pp. 0-10
Author(s):  
Peng-Xu Ding ◽  
Xin-Wei Han ◽  
Chao Liu

Budd-Chiari syndrome (BCS) is a heterogeneous group of disorders characterized by hepatic venous outflow obstruction. Abernethy malformation is a congenital vascular malformation defined by diversion of portal blood away from the liver. Both conditions are rare vascular diseases. We report here the first case of a patient with combined type II Abernethy malformation and Budd-Chiari syndrome from China. The inferior vena cava obstruction was treated with percutaneous balloon angioplasty; close follow-up was elected for the Abernethy malformation.


2021 ◽  
Vol 6 (4) ◽  
pp. 237-240
Author(s):  
Ramakrishna Rachakonda ◽  
Shaik Umar Pasha ◽  
Shaik Abdul Waseem ◽  
Nagarjuna Reddy Sunkara ◽  
Seenu Ayyakannu

A twenty years old male college student came with history of hemoptysis. His chest X-ray showed diffuse infiltrative shadows and he was diagnosed as a case of a case of pulmonary tuberculosis with hemoptysis. On detailed investigations he was found to have Abernethy malformation Type-II with primitive portal vein joining extrahepatic inferior vanacava leading to cirrhosis of liver, porto-pulmonary syndrome, pulmonary arterial hypertension and hemoptysis.


2019 ◽  
Author(s):  
Chen Guo ◽  
Yumin Zhong ◽  
Qian Wang ◽  
Liwei Hu ◽  
Xiaohong Gu ◽  
...  

Abstract Background :Abernethy malformation is a rare congenital abnormality. Imaging examination is an important method for the diagnosis. The purpose of this study was to demonstrate manifestations of multi-slice computed tomography (MSCT) in Abernethy malformation and its diagnostic accuracy. Methods :Fourteen children with Abernethy malformation were admitted to our center in China between July 2011 and January 2018. All 14 patients (eight males and six females) received MSCT and digital subtraction angiography (DSA) while eight patients also received ultrasound. The patients’ age ranged from 1 to 14 (median age 8 years old). The clinical records of the patients were retrospectively reviewed. MSCT raw data were transferred to an Advantage Windows 4.2 or 4.6 workstation (General Electric Medical Systems, Waukesha, WI). We compared the findings of MSCT with DSA and surgical results in order to ascertain diagnostic accuracy. Results :Three cases had type Ib Abernethy malformation and eleven cases had type II. Two cases of type II Abernethy malformation were misdiagnosed as type Ib using MSCT. Comparing the findings of MSCT with DSA and surgical results, the accuracy of MSCT was 85.7% (12/14), in which 100.0% (3/3) were type Ib and 81.8% (9/11) were type II. Clinical information included congenital heart disease, pulmonary hypertension, diffuse pulmonary arteriovenous fistula, abnormal liver function, hepatic nodules, elevated blood ammonia, and hepatic encephalopathy. Eleven cases were treated after diagnosis. One patient with Abernethy malformation type Ib(1/3) underwent liver transplantation. Seven patients with Abernethy malformation type II (7/11) were treated by shunt occlusion, received laparoscopy, or were treated with open surgical ligation. Another three patients (3/11) with Abernethy malformation type II were treated by interventional portocaval shunt occlusion under DSA. Conclusion :MSCT attains excellent capability in diagnosing type II Abernethy malformation and further shows the location of the portacaval shunt. DSA can help when it is hard to determine diagnosis between Abernethy type Ib and II using MSCT. Key words: Abernethy malformation; Angiography; Tomography


2018 ◽  
Vol 53 ◽  
pp. 268.e1-268.e6 ◽  
Author(s):  
Jin-Shan Zhang ◽  
Long Li ◽  
Wei Cheng ◽  
Wen-Ying Hou

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