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  3. tMCS Causing Myocardial Extramedullary Hematopoiesis Secondary to Massive Hemolysis.
 

tMCS Causing Myocardial Extramedullary Hematopoiesis Secondary to Massive Hemolysis.

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BORIS DOI
10.48620/85764
Date of Publication
February 5, 2025
Publication Type
Article
Division/Institute

Clinic of Cardiology

Clinic of Haematology...

Institute of Tissue M...

Contributor
Rothenberger, Raphael
Clinic of Cardiology
Banz, Yaraorcid-logo
Institute of Tissue Medicine and Pathology, Clinical Pathology
Institute of Tissue Medicine and Pathology
Bruno, Jolie Donna
Clinic of Cardiology
Capek, Lukas
Clinic of Cardiology
Fürholz, Monika
Clinic of Cardiology
Neagoe, Alexandra-Maria
Clinic of Cardiology
Hunziker, Lukas
Clinic of Cardiology
Martinelli, Michele
Clinic of Cardiology
Schnegg, Bruno
Clinic of Cardiology
Schnegg-Kaufmann, Annatina
Clinic of Haematology and Central Haematological Laboratory
Subject(s)

600 - Technology::610...

Series
JACC. Case reports.
ISSN or ISBN (if monograph)
2666-0849
Language
English
Publisher DOI
10.1016/j.jaccas.2024.103127
PubMed ID
39963225
Uncontrolled Keywords

acute heart failure

blood

cardiac assist device...

cardiac transplant

complication

dysplasia

imaging

treatment

Description
In 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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/205845
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S2666084924011914-main.pdftextAdobe PDF1.62 MBAttribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0)publishedOpen
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