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Submitted: 16 Apr 2021
Revision: 13 Jan 2022
Accepted: 05 Feb 2022
ePublished: 06 Apr 2022
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J Cardiovasc Thorac Res. 2022;14(2): 144-146.
doi: 10.34172/jcvtr.2022.11
PMID: 35935382
PMCID: PMC9339736
  Abstract View: 649
  PDF Download: 368
  Full Text View: 90

Case Report

Esophageal Intramural Haematoma related Dysphagia: A rare complication after thrombolysis

Samman Verma 1 ORCID logo, Prashant Gupta 1, Amitava Dutta 2, Pankaj Gupta 3, Vishal Sharma 2* ORCID logo

1 Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India
2 Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India
3 Department of Radiodiagnosis, Post Graduate Institute of Medical Education and Research, Chandigarh, India
*Corresponding Author: Corresponding Author: Vishal Sharma, Email: , Email: docvishalsharma@gmail.com

Abstract

Esophageal Intramural Haematoma (EIH) is a rare entity usually caused by repeated emesis or trauma. It is diagnosed on the basis of upper gastrointestinal endoscopy and radiology. Treatment is conservative unless hemodynamic instability prevails. Use of anticoagulation or thrombolytic therapy is believed to be a risk factor rather than a causative etiology. However, a review of literature shows only few cases occurring post-thrombolysis. We report about a patient of myocardial infarction who was thrombolyzed with streptokinase. He developed hematemesis and dysphagia a few hours after thrombolysis despite ECG resolution of his ST elevation. He was diagnosed to have EIH on basis of endoscopic and computed tomographic findings. His symptoms improved within two weeks, and a repeat UGIE showed resolution of the hematoma.
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