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Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome
The incidence of pediatric acute inflammatory gallbladder (GB) disease without gallstone such as acute acalculous cholecystitis has increased with the development of improved diagnostic modalities. Although Epstein–Barr virus (EBV) infection is common in general population, only few cases of GB dise...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504559/ https://www.ncbi.nlm.nih.gov/pubmed/26166109 http://dx.doi.org/10.1097/MD.0000000000001120 |
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author | Yi, Dae Yong Kim, Ji Young Yang, Hye Ran |
author_facet | Yi, Dae Yong Kim, Ji Young Yang, Hye Ran |
author_sort | Yi, Dae Yong |
collection | PubMed |
description | The incidence of pediatric acute inflammatory gallbladder (GB) disease without gallstone such as acute acalculous cholecystitis has increased with the development of improved diagnostic modalities. Although Epstein–Barr virus (EBV) infection is common in general population, only few cases of GB diseases caused by EBV infection have been reported. This study analyzed ultrasonographic characteristics of primary EBV infection in children and evaluated the influence of EBV-associated GB disease on clinical course and outcome of EBV infection. Between March 2004 and January 2013, 94 of 287 pediatric patients with EBV infection underwent abdominal ultrasonography (USG); clinical features, laboratory data, and USG findings were collected and analyzed retrospectively. Of 94 children, ultrasonographic thick GB wall was observed in 24 (25.3%). Platelet counts were lower in the thickened GB wall group than in the normal GB wall thickness group (P = 0.004). Direct bilirubin, alanine aminotransferase, and γ-glutamyl transferase levels were higher in the thickened GB wall group (P = 0.000, P = 0.041, and P = 0.001, respectively). The duration of hospitalization was longer in patients with thickened GB wall (P = 0.043). Radiologic findings of acute acalculous inflammatory GB disease such as thickened GB wall caused by primary EBV infection are more common than previously reported. Consideration of EBV infection in the differential diagnosis of children suspected with acute acalculous GB diseases may avoid unnecessary surgical intervention. |
format | Online Article Text |
id | pubmed-4504559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-45045592015-08-05 Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome Yi, Dae Yong Kim, Ji Young Yang, Hye Ran Medicine (Baltimore) 6200 The incidence of pediatric acute inflammatory gallbladder (GB) disease without gallstone such as acute acalculous cholecystitis has increased with the development of improved diagnostic modalities. Although Epstein–Barr virus (EBV) infection is common in general population, only few cases of GB diseases caused by EBV infection have been reported. This study analyzed ultrasonographic characteristics of primary EBV infection in children and evaluated the influence of EBV-associated GB disease on clinical course and outcome of EBV infection. Between March 2004 and January 2013, 94 of 287 pediatric patients with EBV infection underwent abdominal ultrasonography (USG); clinical features, laboratory data, and USG findings were collected and analyzed retrospectively. Of 94 children, ultrasonographic thick GB wall was observed in 24 (25.3%). Platelet counts were lower in the thickened GB wall group than in the normal GB wall thickness group (P = 0.004). Direct bilirubin, alanine aminotransferase, and γ-glutamyl transferase levels were higher in the thickened GB wall group (P = 0.000, P = 0.041, and P = 0.001, respectively). The duration of hospitalization was longer in patients with thickened GB wall (P = 0.043). Radiologic findings of acute acalculous inflammatory GB disease such as thickened GB wall caused by primary EBV infection are more common than previously reported. Consideration of EBV infection in the differential diagnosis of children suspected with acute acalculous GB diseases may avoid unnecessary surgical intervention. Wolters Kluwer Health 2015-07-13 /pmc/articles/PMC4504559/ /pubmed/26166109 http://dx.doi.org/10.1097/MD.0000000000001120 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6200 Yi, Dae Yong Kim, Ji Young Yang, Hye Ran Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome |
title | Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome |
title_full | Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome |
title_fullStr | Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome |
title_full_unstemmed | Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome |
title_short | Ultrasonographic Gallbladder Abnormality of Primary Epstein–Barr Virus Infection in Children and Its Influence on Clinical Outcome |
title_sort | ultrasonographic gallbladder abnormality of primary epstein–barr virus infection in children and its influence on clinical outcome |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504559/ https://www.ncbi.nlm.nih.gov/pubmed/26166109 http://dx.doi.org/10.1097/MD.0000000000001120 |
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