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Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report
BACKGROUND: Submucosal hematoma (SH) is one of the rare causes of upper gastrointestinal bleeding. As a rare and critical disease in clinical practice, it should be paid more attention to by clinicians to avoid missed diagnosis and misdiagnosis. Most of the esophageal submucosal hematomas have clear...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281432/ https://www.ncbi.nlm.nih.gov/pubmed/34307625 http://dx.doi.org/10.12998/wjcc.v9.i20.5683 |
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author | Liu, Liang Shen, Xing-Jie Xue, Li-Jun Yao, Shu-Kun Zhu, Jing-Yu |
author_facet | Liu, Liang Shen, Xing-Jie Xue, Li-Jun Yao, Shu-Kun Zhu, Jing-Yu |
author_sort | Liu, Liang |
collection | PubMed |
description | BACKGROUND: Submucosal hematoma (SH) is one of the rare causes of upper gastrointestinal bleeding. As a rare and critical disease in clinical practice, it should be paid more attention to by clinicians to avoid missed diagnosis and misdiagnosis. Most of the esophageal submucosal hematomas have clear causes, including retrosternal pain, dysphagia, etc. Here, we report a rare case of SH extending from the hypopharynx to the lower esophagus caused by oral administration of hirudin and panax notoginseng powder, with atypical clinical manifestation. Such a long submucosal hematoma has rarely been reported. CASE SUMMARY: The patient was a 60-year-old male with a history of gastritis, hypertension, coronary heart disease, and coronary stent implantation. The patient developed chest tiredness and heartburn after taking 10 capsules of a homemade mixture of hirudin and notoginseng powder in the previous 2 d. He did not have hematemesis or black stool. Gastroscopy and chest computed tomography confirmed the diagnosis of SH, which ranged from the pharynx to the lower esophagus and was 35-40 cm in length. After the diagnosis was confirmed, we performed active conservative treatment on the patient, and the patient recovered well and remained asymptomatic during the 26-mo follow-up. CONCLUSION: SH is rare, and cases with atypical clinical symptoms may lead to misdiagnosis and missed diagnosis. Ignorance of this disease can lead to serious clinical consequences. Conservative therapy is effective and the prognosis is good. |
format | Online Article Text |
id | pubmed-8281432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-82814322021-07-22 Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report Liu, Liang Shen, Xing-Jie Xue, Li-Jun Yao, Shu-Kun Zhu, Jing-Yu World J Clin Cases Case Report BACKGROUND: Submucosal hematoma (SH) is one of the rare causes of upper gastrointestinal bleeding. As a rare and critical disease in clinical practice, it should be paid more attention to by clinicians to avoid missed diagnosis and misdiagnosis. Most of the esophageal submucosal hematomas have clear causes, including retrosternal pain, dysphagia, etc. Here, we report a rare case of SH extending from the hypopharynx to the lower esophagus caused by oral administration of hirudin and panax notoginseng powder, with atypical clinical manifestation. Such a long submucosal hematoma has rarely been reported. CASE SUMMARY: The patient was a 60-year-old male with a history of gastritis, hypertension, coronary heart disease, and coronary stent implantation. The patient developed chest tiredness and heartburn after taking 10 capsules of a homemade mixture of hirudin and notoginseng powder in the previous 2 d. He did not have hematemesis or black stool. Gastroscopy and chest computed tomography confirmed the diagnosis of SH, which ranged from the pharynx to the lower esophagus and was 35-40 cm in length. After the diagnosis was confirmed, we performed active conservative treatment on the patient, and the patient recovered well and remained asymptomatic during the 26-mo follow-up. CONCLUSION: SH is rare, and cases with atypical clinical symptoms may lead to misdiagnosis and missed diagnosis. Ignorance of this disease can lead to serious clinical consequences. Conservative therapy is effective and the prognosis is good. Baishideng Publishing Group Inc 2021-07-16 2021-07-16 /pmc/articles/PMC8281432/ /pubmed/34307625 http://dx.doi.org/10.12998/wjcc.v9.i20.5683 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Liu, Liang Shen, Xing-Jie Xue, Li-Jun Yao, Shu-Kun Zhu, Jing-Yu Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report |
title | Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report |
title_full | Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report |
title_fullStr | Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report |
title_full_unstemmed | Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report |
title_short | Submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: A case report |
title_sort | submucosal hematoma with a wide range of lesions, severe condition and atypical clinical symptoms: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281432/ https://www.ncbi.nlm.nih.gov/pubmed/34307625 http://dx.doi.org/10.12998/wjcc.v9.i20.5683 |
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