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A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging

INTRODUCTION: Spontaneous mesenteric hematoma is an uncommon syndrome triggered by bleeding localized in the mesenteric vascular tree of a bowel segment for no apparent underlying reason. We herein report a surgical patient with an extremely rapidly growing spontaneous mesenteric hematoma that we su...

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Autores principales: Nakamura, Shunsuke, Yamada, Taihei, Nojima, Tsuyoshi, Naito, Hiromichi, Koga, Hitoshi, Yamashita, Hisashi, Gochi, Akira, Nakao, Atsunori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849124/
https://www.ncbi.nlm.nih.gov/pubmed/31715445
http://dx.doi.org/10.1016/j.ijscr.2019.10.058
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author Nakamura, Shunsuke
Yamada, Taihei
Nojima, Tsuyoshi
Naito, Hiromichi
Koga, Hitoshi
Yamashita, Hisashi
Gochi, Akira
Nakao, Atsunori
author_facet Nakamura, Shunsuke
Yamada, Taihei
Nojima, Tsuyoshi
Naito, Hiromichi
Koga, Hitoshi
Yamashita, Hisashi
Gochi, Akira
Nakao, Atsunori
author_sort Nakamura, Shunsuke
collection PubMed
description INTRODUCTION: Spontaneous mesenteric hematoma is an uncommon syndrome triggered by bleeding localized in the mesenteric vascular tree of a bowel segment for no apparent underlying reason. We herein report a surgical patient with an extremely rapidly growing spontaneous mesenteric hematoma that we successfully diagnosed using careful radiologic examination. PRESENTATION OF CASE: A 56-year-old old male presenting sudden onset lower abdominal pain was referred to our emergency department. At the time of admission, his physical examination revealed stable vital signs without radiological abnormality. On the following day, the patient suddenly presented hypotension, tachycardia, and increased abdominal pain. Contrast-enhanced computed tomography examination showed a mass with both high- and low-density areas with a 130 mm maximum diameter bordering the transverse colon. Since interventional radiologists were not available, we decided to perform emergency exploratory laparotomy. On laparotomy, a 13 × 8 cm hematoma was found in the mesentery of the transverse colon. As bleeding was noted from the branches of the middle colic artery and gastrocolic artery, these responsible vessels were ligated. The patient was finally given the diagnosis of spontaneous mesenteric hematoma. DISCUSSION AND CONCLUSION: The present case, initially diagnosed as enterocolitis, suddenly manifested hypovolemic shock. Close monitoring for any signs of further deterioration, as well as aggressive imaging diagnosis, enabled us to avoid delays in treatment. Early diagnosis and treatment of mesenteric hematomas are essential to prevent them from rupturing and triggering life-threatening adverse events.
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spelling pubmed-68491242019-11-15 A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging Nakamura, Shunsuke Yamada, Taihei Nojima, Tsuyoshi Naito, Hiromichi Koga, Hitoshi Yamashita, Hisashi Gochi, Akira Nakao, Atsunori Int J Surg Case Rep Article INTRODUCTION: Spontaneous mesenteric hematoma is an uncommon syndrome triggered by bleeding localized in the mesenteric vascular tree of a bowel segment for no apparent underlying reason. We herein report a surgical patient with an extremely rapidly growing spontaneous mesenteric hematoma that we successfully diagnosed using careful radiologic examination. PRESENTATION OF CASE: A 56-year-old old male presenting sudden onset lower abdominal pain was referred to our emergency department. At the time of admission, his physical examination revealed stable vital signs without radiological abnormality. On the following day, the patient suddenly presented hypotension, tachycardia, and increased abdominal pain. Contrast-enhanced computed tomography examination showed a mass with both high- and low-density areas with a 130 mm maximum diameter bordering the transverse colon. Since interventional radiologists were not available, we decided to perform emergency exploratory laparotomy. On laparotomy, a 13 × 8 cm hematoma was found in the mesentery of the transverse colon. As bleeding was noted from the branches of the middle colic artery and gastrocolic artery, these responsible vessels were ligated. The patient was finally given the diagnosis of spontaneous mesenteric hematoma. DISCUSSION AND CONCLUSION: The present case, initially diagnosed as enterocolitis, suddenly manifested hypovolemic shock. Close monitoring for any signs of further deterioration, as well as aggressive imaging diagnosis, enabled us to avoid delays in treatment. Early diagnosis and treatment of mesenteric hematomas are essential to prevent them from rupturing and triggering life-threatening adverse events. Elsevier 2019-10-31 /pmc/articles/PMC6849124/ /pubmed/31715445 http://dx.doi.org/10.1016/j.ijscr.2019.10.058 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nakamura, Shunsuke
Yamada, Taihei
Nojima, Tsuyoshi
Naito, Hiromichi
Koga, Hitoshi
Yamashita, Hisashi
Gochi, Akira
Nakao, Atsunori
A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
title A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
title_full A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
title_fullStr A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
title_full_unstemmed A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
title_short A case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
title_sort case of spontaneous mesenteric hematoma successfully diagnosed and treated with aggressive imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849124/
https://www.ncbi.nlm.nih.gov/pubmed/31715445
http://dx.doi.org/10.1016/j.ijscr.2019.10.058
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