Spontaneous rupture of the oesophagus: endoscopic treatment in the primary stage.

نویسندگان

  • R A Härmä
  • Y O Koskinen
  • S O Suurkari
چکیده

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Spontaneous Rupture of the Oesophagus: Boerhaaves Syndrome in 2008

Objective: Boerhaave’s syndrome is a spontaneous rupture of the oesophagus with a lack of diagnostic and treatment consistency in the literature. Therefore, we reviewed all published literature in order to design a treatment algorithm based on the literature. Study Design: A systematic literature review written in the English language since 1975. Results: We reviewed all known literature. Treat...

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Spontaneous dissection of the oesophagus.

Spontaneous rupture of the oesophagus is a well-known entity. Partial or intramural rupture of the oesophagus has been described but is not so well known, and the purpose of this paper is to draw attention to this condition. The clinical presentation, radiological appearances, and treatment of two such cases are described.

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A Case of Non-familial Degenerative Chorea.

BARRETr, N. P. (1946): Spontaneous Rupture of the Oesophagus-Review of the Literature and Report of 3 cases, Thorax, 48, 1. BARRETT, N. P. (1947): Report of a Case of Spontaneous Rupture of the Oesophagus successfully treated by Operation, Brit. J. Surg., 216, 35. BEAL, J. M. (1949): Spontaneous Rupture of the Oesophagus, Ann. Surg., 129, 572. BUNCH, G. H. (Jr.) (1957): Spontaneous Rupture of t...

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A case with bilateral spontaneous pneumothorax was presented. Etiology, mechanism, and treatment were discussed on the review of literature. Spontaneous Pneumothorax is a clinical entity resulting from a sudden non traumatic rupture of the lung. Biach reported in 1880 that 78% of 916 patients with spontaneous pneumothorax had tuberculosis. Kjergaard emphasized 1932 the primary importance of sub...

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An Atypical Case of Spontaneous Rupture of the Oesophagus

A case of spontaneous rupture of the oesophagus is described in which the presentation is unusual. The rarity of the condition is emphasized. The diagnosis and treatment are briefly considered and the difficulties in diagnosis stressed. The similarities and differences between this condition and the Mallory-Weiss syndrome are discussed.

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عنوان ژورنال:
  • Thorax

دوره 23 2  شماره 

صفحات  -

تاریخ انتشار 1968