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Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child
Accessory hepatic lobe is noted as and considered a rare disease in children. It can manifest with various symptoms and complications depending on the location, volume, type and position of the disease as presented on a child. The patient presented as a 14-month-old girl who was seen with a notable...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182474/ https://www.ncbi.nlm.nih.gov/pubmed/30345253 http://dx.doi.org/10.5223/pghn.2018.21.4.361 |
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author | Sağ, Elif Cansu, Ayşegül İmamoğlu, Mustafa Çakır, Murat |
author_facet | Sağ, Elif Cansu, Ayşegül İmamoğlu, Mustafa Çakır, Murat |
author_sort | Sağ, Elif |
collection | PubMed |
description | Accessory hepatic lobe is noted as and considered a rare disease in children. It can manifest with various symptoms and complications depending on the location, volume, type and position of the disease as presented on a child. The patient presented as a 14-month-old girl who was seen with a notable hepatosplenomegaly and portal hypertension. A diagnosis was made after taking an extensive medical history, observation and radiological examinations. The formal diagnosis was a prehepatic portal hypertension associated with accessory hepatic lobe. |
format | Online Article Text |
id | pubmed-6182474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-61824742018-10-19 Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child Sağ, Elif Cansu, Ayşegül İmamoğlu, Mustafa Çakır, Murat Pediatr Gastroenterol Hepatol Nutr Case Report Accessory hepatic lobe is noted as and considered a rare disease in children. It can manifest with various symptoms and complications depending on the location, volume, type and position of the disease as presented on a child. The patient presented as a 14-month-old girl who was seen with a notable hepatosplenomegaly and portal hypertension. A diagnosis was made after taking an extensive medical history, observation and radiological examinations. The formal diagnosis was a prehepatic portal hypertension associated with accessory hepatic lobe. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2018-10 2018-10-10 /pmc/articles/PMC6182474/ /pubmed/30345253 http://dx.doi.org/10.5223/pghn.2018.21.4.361 Text en Copyright © 2018 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Sağ, Elif Cansu, Ayşegül İmamoğlu, Mustafa Çakır, Murat Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child |
title | Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child |
title_full | Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child |
title_fullStr | Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child |
title_full_unstemmed | Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child |
title_short | Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child |
title_sort | accessory hepatic lobe: a rare cause of prehepatic portal hypertension in a child |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182474/ https://www.ncbi.nlm.nih.gov/pubmed/30345253 http://dx.doi.org/10.5223/pghn.2018.21.4.361 |
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