Publication:
Infective endocarditis on interventricular communication as cause of massive haemoptysis: a case report.

dc.contributor.authorRodríguez Torres, Diego José
dc.contributor.authorRodríguez, Diego Segura
dc.contributor.authorEscobar, Eduardo Moreno
dc.contributor.authorOrta, Rocío García
dc.date.accessioned2023-05-03T13:27:24Z
dc.date.available2023-05-03T13:27:24Z
dc.date.issued2022-09-05
dc.description.abstractHaemoptysis is a rare symptom associated with endocarditis. We describe the unusual clinical manifestation of endocarditis on regurgitant bicuspid aortic valve and (probably) secondarily on a perimembranous ventricular septal defect (VSD) as massive haemoptysis. A 24-year-old male with aortic coarctation, bicuspid aortic valve, and VSD since birth. Previously asymptomatic, he came after an episode of haemoptysis. A computed tomography (CT) scan showed a cavitated lesion in lung. Streptococo viridans was identified in serial blood cultures. Transthoracic echocardiography showed a bicuspid aortic valve with vegetations, suggesting infectious involvement, and severe aortic insufficiency. Transoesophageal echocardiography (TEE) study showed a bicuspid aortic valve with complete fusion of coronary valves. An elongated oscillating tumour, 9.5 mm in length, was observed in the centre of the ventricular side of the non-coronary valve. Another vegetation was seen on the VSD. During his hospital stay and under antibiotic treatment, he reported abdominal pain. Computed tomography examination showed splenic infarction. In the echocardiogram no vegetation masses were observed on the aortic valve or on the VSD closure aneurysm. The main debate about this patient's treatment concerned the indication of surgery, especially after the onset of fever with splenic septic embolism while under appropriate antibiotic treatment. He was stable, with no signs of heart failure and the echocardiogram repeated after the septic splenic embolism showed no residual vegetations on the aortic valve or VSD, and the TEE study ruled out a local complication. Finally, the multidisciplinary team decided against surgical management.
dc.identifier.doi10.1093/ehjcr/ytac350
dc.identifier.essn2514-2119
dc.identifier.pmcPMC9467288
dc.identifier.pmid36106132
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467288/pdf
dc.identifier.unpaywallURLhttps://academic.oup.com/ehjcr/article-pdf/6/9/ytac350/45804080/ytac350.pdf
dc.identifier.urihttp://hdl.handle.net/10668/19761
dc.issue.number9
dc.journal.titleEuropean heart journal. Case reports
dc.journal.titleabbreviationEur Heart J Case Rep
dc.language.isoen
dc.organizationHospital Universitario San Cecilio
dc.organizationHospital Universitario San Cecilio
dc.organizationHospital Universitario Virgen de las Nieves
dc.page.numberytac350
dc.pubmedtypeCase Reports
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectCase report
dc.subjectCongenital heart malformation
dc.subjectEndocarditis
dc.subjectHaemoptysis
dc.titleInfective endocarditis on interventricular communication as cause of massive haemoptysis: a case report.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number6
dspace.entity.typePublication

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