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Dual pathology—An unreported case

INTRODUCTION: Symptomatic biliary disease in children and young adults requiring surgical intervention are uncommon. However even rarer is the occurrence of a spontaneous gallbladder necrosis in a child. We report a case of spontaneous necrosis in a child with no apparent causative factors. CASE: Fi...

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Autores principales: Yap, Darren, Rasheed, Ashraf, Rashid, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701805/
https://www.ncbi.nlm.nih.gov/pubmed/26657530
http://dx.doi.org/10.1016/j.ijscr.2015.11.002
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author Yap, Darren
Rasheed, Ashraf
Rashid, Majid
author_facet Yap, Darren
Rasheed, Ashraf
Rashid, Majid
author_sort Yap, Darren
collection PubMed
description INTRODUCTION: Symptomatic biliary disease in children and young adults requiring surgical intervention are uncommon. However even rarer is the occurrence of a spontaneous gallbladder necrosis in a child. We report a case of spontaneous necrosis in a child with no apparent causative factors. CASE: Fit and well 16 year-old boy presented with acute generalized lower abdominal pain. Examination revealed mild epigastric pain with rebound tenderness and guarding of the right iliac fossa. Diagnostic laparoscopy showed a necrotic gallbladder and incidental finding of a Meckel’s diverticulum. He had a cholecystectomy and Meckel’s diverticulum resection. Patient recovered uneventfully and was discharged home. He was reviewed 2 months later and recovered well with no evidence of any post-operative complication. He was discharged without any further follow up. DISCUSSION: Gall bladder necrosis is a rare cause of an acute abdomen. We present the first reported case of a spontaneous gallbladder necrosis with no apparent cause. Literature review showed various causes of gall bladder necrosis including trauma, acalculous cholecystitis, gallbladder torsion, gangrenous cholecystitis and etc. CONCLUSION: We report a case of spontaneous gallbladder necrosis in a young healthy male with no family history of thrombotic disorders or any history of sepsis, intervention, trauma and no obvious underlying anatomical or histological abnormalities. This is an exceedingly rare pathology and one would be forgiven for not including it on the list of a differential diagnosis in such circumstance. However it is important to send tissue sample to exclude any underlying histological aetiological factors.
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spelling pubmed-47018052016-02-03 Dual pathology—An unreported case Yap, Darren Rasheed, Ashraf Rashid, Majid Int J Surg Case Rep Case Report INTRODUCTION: Symptomatic biliary disease in children and young adults requiring surgical intervention are uncommon. However even rarer is the occurrence of a spontaneous gallbladder necrosis in a child. We report a case of spontaneous necrosis in a child with no apparent causative factors. CASE: Fit and well 16 year-old boy presented with acute generalized lower abdominal pain. Examination revealed mild epigastric pain with rebound tenderness and guarding of the right iliac fossa. Diagnostic laparoscopy showed a necrotic gallbladder and incidental finding of a Meckel’s diverticulum. He had a cholecystectomy and Meckel’s diverticulum resection. Patient recovered uneventfully and was discharged home. He was reviewed 2 months later and recovered well with no evidence of any post-operative complication. He was discharged without any further follow up. DISCUSSION: Gall bladder necrosis is a rare cause of an acute abdomen. We present the first reported case of a spontaneous gallbladder necrosis with no apparent cause. Literature review showed various causes of gall bladder necrosis including trauma, acalculous cholecystitis, gallbladder torsion, gangrenous cholecystitis and etc. CONCLUSION: We report a case of spontaneous gallbladder necrosis in a young healthy male with no family history of thrombotic disorders or any history of sepsis, intervention, trauma and no obvious underlying anatomical or histological abnormalities. This is an exceedingly rare pathology and one would be forgiven for not including it on the list of a differential diagnosis in such circumstance. However it is important to send tissue sample to exclude any underlying histological aetiological factors. Elsevier 2015-12-01 /pmc/articles/PMC4701805/ /pubmed/26657530 http://dx.doi.org/10.1016/j.ijscr.2015.11.002 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yap, Darren
Rasheed, Ashraf
Rashid, Majid
Dual pathology—An unreported case
title Dual pathology—An unreported case
title_full Dual pathology—An unreported case
title_fullStr Dual pathology—An unreported case
title_full_unstemmed Dual pathology—An unreported case
title_short Dual pathology—An unreported case
title_sort dual pathology—an unreported case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701805/
https://www.ncbi.nlm.nih.gov/pubmed/26657530
http://dx.doi.org/10.1016/j.ijscr.2015.11.002
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