Literature DB >> 23245671

Abernethy malformation type II with nephrotic syndrome and other multisystemic presentation: an illustrative case for understanding pathogenesis of extrahepatic complication of congenital portosystemic shunt.

David F Schaeffer1, Simin Laiq, Hyun-Jung Jang, Rohan John, Oyedele A Adeyi.   

Abstract

Abernethy malformation, an extrahepatic congenital portosystemic shunt, is more often diagnosed based on associated cardiac or pulmonary malformation. Although predominately a pediatric diagnosis, "late diagnoses" in adulthood have been reported especially in type II malformations that involve only a partial shunt of portal circulation directly into the inferior vena cava. Aside from the cardiac-related presentation, Abernethy malformation is also associated with multiple liver nodules, either benign or malignant, and pulmonary hypertension. In this report, we present immunoglobulin A glomerulonephritis with nephrotic syndrome as a hitherto unrecognized manifestation of this malformation outside the pediatric population, in a patient who also had pulmonary hypertension and multiple liver tumors. We also propose a pathogenetic basis for this multisystemic presentation that includes release into the systemic circulation of unfiltered bacteria, vasoactive substances, and immunoglobulin A-antigen complexes.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23245671     DOI: 10.1016/j.humpath.2012.08.018

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  7 in total

Review 1.  Vascular patterning sets the stage for macro and micro hepatic architecture.

Authors:  Ashley E Cast; Teagan J Walter; Stacey S Huppert
Journal:  Dev Dyn       Date:  2014-11-18       Impact factor: 3.780

2.  Congenital absence of the portal vein associated with focal nodular hyperplasia of the liver and congenital heart disease (Abernethy malformation): A case report and literature review.

Authors:  Yabin Hao; Xu Hong; Xinyan Zhao
Journal:  Oncol Lett       Date:  2014-12-04       Impact factor: 2.967

3.  Endovascular Closure Resolves Trimethylaminuria Caused by Congenital Portosystemic Shunts.

Authors:  María Dolores Ponce-Dorrego; Gonzalo Garzón-Moll
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2019-11-07

4.  Case Report: Membranoproliferative Glomerulonephritis, a Rare Clinical Manifestation of Abernethy Malformation Type II.

Authors:  Xue He; Yueling Zhu; Haidong Fu; Chunyue Feng; Zhixia Liu; Weizhong Gu; Yanyan Jin; Binbin Yang; Huijun Shen
Journal:  Front Pediatr       Date:  2021-03-17       Impact factor: 3.418

5.  A rare presentation of type II Abernethy malformation and nephrotic syndrome: Case report and review.

Authors:  Xin Wu; Weizhong Gu; Yongzhi Lin; Lina Ye
Journal:  Open Life Sci       Date:  2022-07-21       Impact factor: 1.311

6.  Significance of CT scan and color Doppler duplex ultrasound in the assessment of Abernethy malformation.

Authors:  Lucas Souto Nacif; Denise Cerqueira Paranaguá-Vezozzo; Flávio Henrique Ferreira Galvão; Manoel S Rocha; Wellington Andraus; Flair Jose Carrilho; Luiz Carneiro D'Albuquerque
Journal:  BMC Med Imaging       Date:  2015-09-18       Impact factor: 1.930

7.  Case Report: A Rare Syncope Case Caused by Abernethy II and a Review of the Literature.

Authors:  Xue-Qin Lin; Jing-Yi Rao; Yi-Fei Xiang; Li-Wei Zhang; Xiao-Ling Cai; Yan-Song Guo; Kai-Yang Lin
Journal:  Front Cardiovasc Med       Date:  2022-01-04
  7 in total

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