The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment

dc.contributor.authorClain, David Jocelynen_ZA
dc.date.accessioned2017-12-07T08:05:01Z
dc.date.available2017-12-07T08:05:01Z
dc.date.issued1968en_ZA
dc.date.updated2017-08-08T09:02:25Z
dc.description.abstractSymptomatic occlusion of the hepatic veins is a rare condition caused by tumour or thrombus arising either locally or by extension from the inferior vena cava. It is usually called the Budd-Chiari syndrome. The etiology remains unknown in over two-thirds of the patients. Its rarity and interest has led to a large number of individual case reports. 322 instances of symptomatic hepatic vein occlusion have been reported, of which 184 are single case publications. There are only six series of more than five cases (Nishikawa, 1910; Corinini and Oberson. 1937; Palnar, 1954; Parker, 1959; Gibson, 1960; Safouh and Shehata, 1965) and these have been largely drawn from autopsy records, although Palmer (1954) described seven patients seen during life. The clinical and pathological features of hepatic vein occlusion have been described in a number of papers (Hess, 1905; Thompson and Turnbull, 1912; Armstrong and Carnes, 1944; Kelsey and Comfort, 1945; Thompson, 1947; Parker, 1959; Gibson, 1960) during the one hundred and twenty years since the publication of Budd's treatise. However, accurate diagnosis has generally relied on autopsy, and detailed investigations have seldom been performed. Consequently, little is known of the roentgenographic and haemodynamic features. The diagnosis of liver disease has been revolutionized by such special techniques as percutaneous liver biopsy, portal pressure measurements, isotope scanning and selective arteriography and venography. This study describes six patients with the Budd-Chiari syndrome in whom these methods have been applied to establish the diagnosis, to ascertain the underlying cause and to assess the possibility of surgical intervention. Special attention has been given to hepatic venography and hepatography. The vascular pattern in the Budd-Chiari syndrome has been compared with that in normals and in patients with other diseases of the liver. Diagnostic features have been determined and an attempt made to evaluate compensatory changes in the lymphatic drainage and venous blood supply following hepatic vein obstruction. Alterations in portal dynamics have also been recorded. The clinical course has been followed and the effect of treatment assessed in each patient. Finally, the literature has been reviewed with particular reference to the diagnosis and treatment of hepatic vein thrombosis. The studies reported in this thesis were carried out during the tenure of a Research Fellowship in the Royal Free Hospital School of Medicine, and they were supported by a grant from the William Shepherd Bequest to the Royal Free Hospital. The special radiological procedures, haemodynamic studies, isotope investigations and laboratory work were personally performed with the exception of the scintillation scans, coeliac axis arteriograms and the other individual tests acknowledged overleaf.en_ZA
dc.identifier.apacitationClain, D. J. (1968). <i>The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment</i>. (Thesis). University of Cape Town ,Faculty of Health Sciences ,UCT/MRC Liver Research Centre. Retrieved from http://hdl.handle.net/11427/26484en_ZA
dc.identifier.chicagocitationClain, David Jocelyn. <i>"The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment."</i> Thesis., University of Cape Town ,Faculty of Health Sciences ,UCT/MRC Liver Research Centre, 1968. http://hdl.handle.net/11427/26484en_ZA
dc.identifier.citationClain, D. 1968. The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment. University of Cape Town.en_ZA
dc.identifier.ris TY - Thesis / Dissertation AU - Clain, David Jocelyn AB - Symptomatic occlusion of the hepatic veins is a rare condition caused by tumour or thrombus arising either locally or by extension from the inferior vena cava. It is usually called the Budd-Chiari syndrome. The etiology remains unknown in over two-thirds of the patients. Its rarity and interest has led to a large number of individual case reports. 322 instances of symptomatic hepatic vein occlusion have been reported, of which 184 are single case publications. There are only six series of more than five cases (Nishikawa, 1910; Corinini and Oberson. 1937; Palnar, 1954; Parker, 1959; Gibson, 1960; Safouh and Shehata, 1965) and these have been largely drawn from autopsy records, although Palmer (1954) described seven patients seen during life. The clinical and pathological features of hepatic vein occlusion have been described in a number of papers (Hess, 1905; Thompson and Turnbull, 1912; Armstrong and Carnes, 1944; Kelsey and Comfort, 1945; Thompson, 1947; Parker, 1959; Gibson, 1960) during the one hundred and twenty years since the publication of Budd's treatise. However, accurate diagnosis has generally relied on autopsy, and detailed investigations have seldom been performed. Consequently, little is known of the roentgenographic and haemodynamic features. The diagnosis of liver disease has been revolutionized by such special techniques as percutaneous liver biopsy, portal pressure measurements, isotope scanning and selective arteriography and venography. This study describes six patients with the Budd-Chiari syndrome in whom these methods have been applied to establish the diagnosis, to ascertain the underlying cause and to assess the possibility of surgical intervention. Special attention has been given to hepatic venography and hepatography. The vascular pattern in the Budd-Chiari syndrome has been compared with that in normals and in patients with other diseases of the liver. Diagnostic features have been determined and an attempt made to evaluate compensatory changes in the lymphatic drainage and venous blood supply following hepatic vein obstruction. Alterations in portal dynamics have also been recorded. The clinical course has been followed and the effect of treatment assessed in each patient. Finally, the literature has been reviewed with particular reference to the diagnosis and treatment of hepatic vein thrombosis. The studies reported in this thesis were carried out during the tenure of a Research Fellowship in the Royal Free Hospital School of Medicine, and they were supported by a grant from the William Shepherd Bequest to the Royal Free Hospital. The special radiological procedures, haemodynamic studies, isotope investigations and laboratory work were personally performed with the exception of the scintillation scans, coeliac axis arteriograms and the other individual tests acknowledged overleaf. DA - 1968 DB - OpenUCT DP - University of Cape Town LK - https://open.uct.ac.za PB - University of Cape Town PY - 1968 T1 - The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment TI - The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment UR - http://hdl.handle.net/11427/26484 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/26484
dc.identifier.vancouvercitationClain DJ. The Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatment. [Thesis]. University of Cape Town ,Faculty of Health Sciences ,UCT/MRC Liver Research Centre, 1968 [cited yyyy month dd]. Available from: http://hdl.handle.net/11427/26484en_ZA
dc.language.isoengen_ZA
dc.publisher.departmentUCT/MRC Liver Research Centreen_ZA
dc.publisher.facultyFaculty of Health Sciencesen_ZA
dc.publisher.institutionUniversity of Cape Town
dc.subject.otherHepatic vein thrombosisen_ZA
dc.titleThe Budd-Chiari syndrome : a study of diagnosis, haemodynamics and treatmenten_ZA
dc.typeDoctoral Thesis
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameMDen_ZA
uct.type.filetype
uct.type.filetypeText
uct.type.filetypeImage
uct.type.publicationResearchen_ZA
uct.type.resourceThesisen_ZA
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