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Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study
BACKGROUND: Dengue infection carries a potential risk of death despite stringent management of plasma leak and haemorrhage. It appears that the extent of liver dysfunction determines the outcome. METHODS: We present a postmortem study of five patients, died of dengue shock syndrome who had markedly...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008311/ https://www.ncbi.nlm.nih.gov/pubmed/24628767 http://dx.doi.org/10.1186/1471-2334-14-141 |
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author | Kularatne, SAM Imbulpitiya, IVB Abeysekera, RA Waduge, RN Rajapakse, RPVJ Weerakoon, KGAD |
author_facet | Kularatne, SAM Imbulpitiya, IVB Abeysekera, RA Waduge, RN Rajapakse, RPVJ Weerakoon, KGAD |
author_sort | Kularatne, SAM |
collection | PubMed |
description | BACKGROUND: Dengue infection carries a potential risk of death despite stringent management of plasma leak and haemorrhage. It appears that the extent of liver dysfunction determines the outcome. METHODS: We present a postmortem study of five patients, died of dengue shock syndrome who had markedly elevated liver enzymes and irreparable circulatory failure. RESULTS: All were females with a median age of 46 years (range 20–50 years). All had positive NS1 and IgM. Clinically, one patient developed severe degree of hepatic encephalopathy whilst three patients developed uncontrollable bleeding manifestations. Dengue virus was detected in three liver specimens by reverse transcription PCR. Histology of the liver revealed massive necrosis with haemorrhages in these patients with evidence of micro and macrovesicular steatosis with significant periportal inflammatory infiltrate. No significant ischaemic changes or necrosis was observed in the other organs. CONCLUSIONS: Severe haemorrhagic necrosis of the liver was the cause of death in these patients probably due to direct viral infection. Predilection for severe liver disease remains unknown. Therefore, it is prudent to think beyond plasma leak as the main pathology of dengue infection and attempts should be made to develop other treatment modalities to prevent and manage unforeseen fatal complications of dengue infection. |
format | Online Article Text |
id | pubmed-4008311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40083112014-05-03 Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study Kularatne, SAM Imbulpitiya, IVB Abeysekera, RA Waduge, RN Rajapakse, RPVJ Weerakoon, KGAD BMC Infect Dis Research Article BACKGROUND: Dengue infection carries a potential risk of death despite stringent management of plasma leak and haemorrhage. It appears that the extent of liver dysfunction determines the outcome. METHODS: We present a postmortem study of five patients, died of dengue shock syndrome who had markedly elevated liver enzymes and irreparable circulatory failure. RESULTS: All were females with a median age of 46 years (range 20–50 years). All had positive NS1 and IgM. Clinically, one patient developed severe degree of hepatic encephalopathy whilst three patients developed uncontrollable bleeding manifestations. Dengue virus was detected in three liver specimens by reverse transcription PCR. Histology of the liver revealed massive necrosis with haemorrhages in these patients with evidence of micro and macrovesicular steatosis with significant periportal inflammatory infiltrate. No significant ischaemic changes or necrosis was observed in the other organs. CONCLUSIONS: Severe haemorrhagic necrosis of the liver was the cause of death in these patients probably due to direct viral infection. Predilection for severe liver disease remains unknown. Therefore, it is prudent to think beyond plasma leak as the main pathology of dengue infection and attempts should be made to develop other treatment modalities to prevent and manage unforeseen fatal complications of dengue infection. BioMed Central 2014-03-14 /pmc/articles/PMC4008311/ /pubmed/24628767 http://dx.doi.org/10.1186/1471-2334-14-141 Text en Copyright © 2014 Kularatne et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kularatne, SAM Imbulpitiya, IVB Abeysekera, RA Waduge, RN Rajapakse, RPVJ Weerakoon, KGAD Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
title | Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
title_full | Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
title_fullStr | Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
title_full_unstemmed | Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
title_short | Extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
title_sort | extensive haemorrhagic necrosis of liver is an unpredictable fatal complication in dengue infection: a postmortem study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008311/ https://www.ncbi.nlm.nih.gov/pubmed/24628767 http://dx.doi.org/10.1186/1471-2334-14-141 |
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