Publication:
Two interesting cases of left atrial myxoma

creativeworkseries.issn1812-2027
dc.contributor.authorAlurkar, VM
dc.contributor.authorNeupane, S
dc.date.accessioned2025-08-11T06:53:38Z
dc.date.available2025-08-11T06:53:38Z
dc.date.issued2010
dc.descriptionAlurkar VM 1, Neupane S 2 1Professor, Cardiologist, Head of Department, Internal Medicine, 2 Intern, Manipal Teaching Hospital, Pokhara, Nepal.
dc.description.abstractAbstract Atrial myxoma is the most common type of benign primary heart tumours. Most of these tumours are sporadic in origin occurring at 3rd to 6th decade of life, while hereditary forms do exist. They are mostly found in the left atrium followed by right atrium and ventricles. A left atrial myxoma may present with features of mitral valve obstruction, embolic phenomenon or systemic disease. On diagnosis, prompt surgical removal is necessary which usually gives a complete cure, though recurrences have been reported. We hereby present two cases of solitary left atrial myxoma. Key words: atrial myxoma, echocardiography, tumour impaction
dc.identifier.urihttps://hdl.handle.net/20.500.14572/1409
dc.language.isoen_US
dc.publisherKathmandu University
dc.titleTwo interesting cases of left atrial myxoma
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage82
oaire.citation.startPage80
relation.isJournalIssueOfPublication99e12c9f-0000-4143-94de-485991ac4554
relation.isJournalIssueOfPublication.latestForDiscovery99e12c9f-0000-4143-94de-485991ac4554
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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