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Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review

Duplications of the alimentary tract are very rare. A one-month-old female presented with symptoms of anorexia, vomiting and continuous watery diarrhea. The plain abdominal radiograph showed thickened intestinal wall and signs of small bowel obstruction. The fevers, vomiting, and continuous wartery...

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Detalles Bibliográficos
Autores principales: Kashiwagi, Y., Suzuki, S., Watanabe, K., Nishimata, S., Kawashima, H., Takekuma, K., Hoshika, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667037/
https://www.ncbi.nlm.nih.gov/pubmed/23761993
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author Kashiwagi, Y.
Suzuki, S.
Watanabe, K.
Nishimata, S.
Kawashima, H.
Takekuma, K.
Hoshika, A.
author_facet Kashiwagi, Y.
Suzuki, S.
Watanabe, K.
Nishimata, S.
Kawashima, H.
Takekuma, K.
Hoshika, A.
author_sort Kashiwagi, Y.
collection PubMed
description Duplications of the alimentary tract are very rare. A one-month-old female presented with symptoms of anorexia, vomiting and continuous watery diarrhea. The plain abdominal radiograph showed thickened intestinal wall and signs of small bowel obstruction. The fevers, vomiting, and continuous wartery diarrhea persisted despite antibiotics, and worsened. The patient failed to respond to medical managements, 27 hours after admission, the patient died due to multiple organ failures. The autopsy was performed, small bowel obstruction due to an ileocecal duplication cyst (3 × 3 cm) was recognized. The ileocecal duplication cyst was attached to the ileum which was changed edematous and necrotic. This potential diagnosis should be borne in mind for a patient who complains of abdominal symptoms with an unknown cause, and duplication cyst should be recognized as a fatal cause in infant.
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spelling pubmed-36670372013-06-12 Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review Kashiwagi, Y. Suzuki, S. Watanabe, K. Nishimata, S. Kawashima, H. Takekuma, K. Hoshika, A. Clin Med Insights Pediatr Case Report Duplications of the alimentary tract are very rare. A one-month-old female presented with symptoms of anorexia, vomiting and continuous watery diarrhea. The plain abdominal radiograph showed thickened intestinal wall and signs of small bowel obstruction. The fevers, vomiting, and continuous wartery diarrhea persisted despite antibiotics, and worsened. The patient failed to respond to medical managements, 27 hours after admission, the patient died due to multiple organ failures. The autopsy was performed, small bowel obstruction due to an ileocecal duplication cyst (3 × 3 cm) was recognized. The ileocecal duplication cyst was attached to the ileum which was changed edematous and necrotic. This potential diagnosis should be borne in mind for a patient who complains of abdominal symptoms with an unknown cause, and duplication cyst should be recognized as a fatal cause in infant. Libertas Academica 2010-09-08 /pmc/articles/PMC3667037/ /pubmed/23761993 Text en © 2010 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.
spellingShingle Case Report
Kashiwagi, Y.
Suzuki, S.
Watanabe, K.
Nishimata, S.
Kawashima, H.
Takekuma, K.
Hoshika, A.
Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review
title Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review
title_full Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review
title_fullStr Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review
title_full_unstemmed Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review
title_short Sudden Unexpected Death Associated with Ileocecal Duplication Cyst and Clinical Review
title_sort sudden unexpected death associated with ileocecal duplication cyst and clinical review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667037/
https://www.ncbi.nlm.nih.gov/pubmed/23761993
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