Literature DB >> 24726750

Spontaneous intramedullary hematoma initially mimicking myocardial infarction.

Dong Hoon Lee1, Yoon Hee Choi2.   

Abstract

Spontaneous intramedullary hematoma (IMH) is a rare condition. The initial clinical manifestations are variable. Early symptoms of high thoracic IMH include thoracocervical pain that can be mistaken for emergent cardiopulmonary conditions such as myocardial infarction, pulmonary embolus, and aortic dissection. We report on a 34-year-old man who presented initially with chest pain and radiating pain in both shoulders. He was initially misdiagnosed as having a myocardial infarction and treated with heparin. Two hours after admission, correct diagnosis of IMH was based on the repeated neurologic examination and spine magnetic resonance imaging study. The patient underwent emergency surgical decompression and hematoma removal.We draw the misdiagnosis to the attention of the emergency physicians because early recognition of spontaneous IMH is very important for early surgical decompression to improve the prognosis.

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Year:  2014        PMID: 24726750     DOI: 10.1016/j.ajem.2014.03.002

Source DB:  PubMed          Journal:  Am J Emerg Med        ISSN: 0735-6757            Impact factor:   2.469


  3 in total

1.  Acute Paraplegia due to Thoracic Hematomyelia.

Authors:  Aykut Akpınar; Bahattin Celik; Ihsan Canbek; Ergun Karavelioğlu
Journal:  Case Rep Neurol Med       Date:  2016-07-12

2.  Spontaneous Spinal Intramedullary Hematoma in an Infant: A Rare Entity and a Diagnostic Challenge.

Authors:  Vibhu Shankar Parashar; Priyanka Aswal; Tarun Kumar Gupta; Gaurav Jaiswal
Journal:  J Pediatr Neurosci       Date:  2021-06-25

3.  Spontaneous spinal epidural hematoma masquerading as atypical abdominal pain in a child: A case report.

Authors:  Xueliang Cheng; Yang Qu; Rongpeng Dong; Lili Yang; Mingyang Kang; Jianwu Zhao
Journal:  Medicine (Baltimore)       Date:  2020-08-14       Impact factor: 1.817

  3 in total

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