Abstract
Beta-thalassemia is an inherited blood disorder caused by reduced or absent synthesis of the beta chains of hemoglobin, resulting in decreased hemoglobin production. Symptoms depend on the type of beta-thalassemia ranging from no symptoms to severe illness. Ineffective erythropoiesis leads to a sequence of events responsible for bone marrow expansion, anemia, hemolysis, splenomegaly, increased iron absorption, and sometimes extramedullary hematopoiesis (EMH). We report an interesting case with EMH visualized on FDG-PET/CT and where FDG-PET/CT has also found the focus of a severe infection in a patient with beta-thalassemia.
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Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.
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The study was designed by Sara E. Dahlsgaard-Wallenius. The first draft of the manuscript was written by Sara E. Dahlsgaard-Wallenius, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
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Sara E. Dahlsgaard-Wallenius, Karen Juul-Jensen, Anne Lerberg Nielsen, and Malene Grubbe Hildebrandt declare that they have no competing interests.
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Dahlsgaard-Wallenius, S.E., Juul-Jensen, K., Nielsen, A.L. et al. Extramedullary Hematopoiesis Visualized on FDG-PET/CT in a Patient with Beta-Thalassemia. Nucl Med Mol Imaging 56, 328–330 (2022). https://doi.org/10.1007/s13139-022-00773-3
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DOI: https://doi.org/10.1007/s13139-022-00773-3