Literature DB >> 20935623

Boerhaave's syndrome - rapidly evolving pleural effusion; a radiographic clue.

C D Hingston1, A G Saayman, P J Frost, M P Wise.   

Abstract

Boerhaave's syndrome is the rare and often fatal condition of spontaneous esophageal rupture. Meckler's triad of vomiting, pain and subcutaneous emphysema are characteristic features of Boerhaave's syndrome. When these symptoms are absent, diagnosis is frequently late and often occurs as the result of incidental investigation. This contributes to the observed high morbidity and mortality. Unless specifically considered in the differential diagnosis, this rare disease is frequently overlooked. The authors described the case of a patient in whom the diagnosis was made several days following presentation by observing that a large pleural effusion had evolved rapidly on chest radiographs. This uncommon radiological sign has relatively few causes and prompted a review of the history and diagnosis, followed by the initiation of additional investigations that confirmed Boerhaave's syndrome.

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Year:  2010        PMID: 20935623

Source DB:  PubMed          Journal:  Minerva Anestesiol        ISSN: 0375-9393            Impact factor:   3.051


  4 in total

1.  Right-sided hydropneumothorax as a presenting symptom of Boerhaave's syndrome (spontaneous esophageal rupture).

Authors:  Supannee Rassameehiran; Saranapoom Klomjit; Kenneth Nugent
Journal:  Proc (Bayl Univ Med Cent)       Date:  2015-07

2.  Cytomorphology of Boerhaave's syndrome: A critical value in cytology.

Authors:  Walid E Khalbuss; Shveta Hooda; Manon Auger
Journal:  Cytojournal       Date:  2013-04-30       Impact factor: 2.091

3.  Boerhaave's syndrome - tension hydropneumothorax and rapidly developing hydropneumothorax: two radiographic clues in one case.

Authors:  Lam Nguyen Ho; Ngoc Tran Van; Thuong Vu Le
Journal:  Respirol Case Rep       Date:  2016-05-05

4.  Boerhaave Syndrome Causing Bilateral Empyemas.

Authors:  Divya Chalikonda; Joseph Yoo; Drew Johnson; Christina Tofani
Journal:  ACG Case Rep J       Date:  2019-09-02
  4 in total

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