Publication:
tMCS Causing Myocardial Extramedullary Hematopoiesis Secondary to Massive Hemolysis.

cris.virtual.author-orcid0000-0003-4474-3132
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cris.virtualsource.author-orcid149dd13d-6e82-4d6b-ab5b-24db3872c3d0
cris.virtualsource.author-orcidb25771e8-1837-41c2-baf5-9549e4c48f60
cris.virtualsource.author-orcida5840fa0-abbf-4cd9-85e0-fd2ee62b023c
cris.virtualsource.author-orcidef5e6706-1f9f-4150-a476-233650ee1bcc
datacite.rightsopen.access
dc.contributor.authorRothenberger, Raphael
dc.contributor.authorBanz, Yara
dc.contributor.authorBruno, Jolie Donna
dc.contributor.authorCapek, Lukas
dc.contributor.authorFürholz, Monika
dc.contributor.authorNeagoe, Alexandra-Maria
dc.contributor.authorHunziker, Lukas
dc.contributor.authorMartinelli, Michele
dc.contributor.authorSchnegg, Bruno
dc.contributor.authorSchnegg-Kaufmann, Annatina
dc.date.accessioned2025-03-06T08:15:20Z
dc.date.available2025-03-06T08:15:20Z
dc.date.issued2025-02-05
dc.description.abstractIn severe heart failure with hemodynamic failure, when inotropic therapies no longer suffice (INTERMACS [Interagency Registry for Mechanically Assisted Circulatory Support] 1), temporary mechanical support is used as a bridging measure until a more definitive treatment, such as a left ventricular assist device, a total artificial heart or transplantation, is performed. Due to shear stress during the passage of blood through the pump, limited hemolysis is to be expected. We describe the case of a 37-year-old patient with terminal heart failure who suffered severe hemolysis during treatment with temporary mechanical support. Examination of the cardiac apex after left ventricular assist device implantation revealed a poorly differentiated tumor. Histopathologic examination revealed underlying extramedullary hematopoiesis, triggered by severe hemolytic anemia. Following exclusion of neoplasia, the patient subsequently underwent heart transplantation. Post-transplantation, the patient was diagnosed with alpha-thalassemia and heterozygote hemoglobin E. This combination can result in mild thalassemia with chronic low-level hemolysis and mild anemia, probably severely exacerbated in the presence of high-shear stress.
dc.description.sponsorshipClinic of Cardiology
dc.description.sponsorshipClinic of Haematology and Central Haematological Laboratory
dc.description.sponsorshipInstitute of Tissue Medicine and Pathology, Clinical Pathology
dc.identifier.doi10.48620/85764
dc.identifier.pmid39963225
dc.identifier.publisherDOI10.1016/j.jaccas.2024.103127
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/205845
dc.language.isoen
dc.relation.ispartofJACC. Case reports.
dc.relation.issn2666-0849
dc.subjectacute heart failure
dc.subjectblood
dc.subjectcardiac assist devices
dc.subjectcardiac transplant
dc.subjectcomplication
dc.subjectdysplasia
dc.subjectimaging
dc.subjecttreatment
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titletMCS Causing Myocardial Extramedullary Hematopoiesis Secondary to Massive Hemolysis.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue3
oaire.citation.startPage103127
oaire.citation.volume30
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationInstitute of Tissue Medicine and Pathology, Clinical Pathology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Cardiology
oairecerif.author.affiliationClinic of Haematology and Central Haematological Laboratory
oairecerif.author.affiliation2Institute of Tissue Medicine and Pathology
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unibe.contributor.rolecorresponding author
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unibe.description.ispublishedpub
unibe.refereedtrue
unibe.subtype.articlecontribution

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