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Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis

Background: Red blood cells (RBC) scintigraphy can be used not only for detection of bleeding sites, but also of spleen tissue. However, there is no established quantitative readout. Therefore, we investigated uptake in suspected splenic lesions in direct quantitative correlation to sites of physiol...

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Autores principales: Holzgreve, Adrien, Völter, Friederike, Delker, Astrid, Kunz, Wolfgang G., Fabritius, Matthias P., Brendel, Matthias, Albert, Nathalie L., Bartenstein, Peter, Unterrainer, Marcus, Unterrainer, Lena M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871479/
https://www.ncbi.nlm.nih.gov/pubmed/35204576
http://dx.doi.org/10.3390/diagnostics12020486
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author Holzgreve, Adrien
Völter, Friederike
Delker, Astrid
Kunz, Wolfgang G.
Fabritius, Matthias P.
Brendel, Matthias
Albert, Nathalie L.
Bartenstein, Peter
Unterrainer, Marcus
Unterrainer, Lena M.
author_facet Holzgreve, Adrien
Völter, Friederike
Delker, Astrid
Kunz, Wolfgang G.
Fabritius, Matthias P.
Brendel, Matthias
Albert, Nathalie L.
Bartenstein, Peter
Unterrainer, Marcus
Unterrainer, Lena M.
author_sort Holzgreve, Adrien
collection PubMed
description Background: Red blood cells (RBC) scintigraphy can be used not only for detection of bleeding sites, but also of spleen tissue. However, there is no established quantitative readout. Therefore, we investigated uptake in suspected splenic lesions in direct quantitative correlation to sites of physiologic uptake in order to objectify the readout. Methods: 20 patients with Tc-99m-labelled RBC scintigraphy and SPECT/low-dose CT for assessment of suspected splenic tissue were included. Lesions were rated as vital splenic or non-splenic tissue, and uptake and physiologic uptake of bone marrow, pancreas, and spleen were then quantified using a volume-of-interest based approach. Hepatic uptake served as a reference. Results: The median uptake ratio was significantly higher in splenic (2.82 (range, 0.58–24.10), n = 47) compared to other lesions (0.49 (0.01–0.83), n = 7), p < 0.001, and 5 lesions were newly discovered. The median pancreatic uptake was 0.09 (range 0.03–0.67), bone marrow 0.17 (0.03–0.45), and orthotopic spleen 14.45 (3.04–29.82). Compared to orthotopic spleens, the pancreas showed lowest uptake (0.09 vs. 14.45, p = 0.004). Based on pancreatic uptake we defined a cutoff (0.75) to distinguish splenic from other tissues. Conclusion: As the uptake in extra-splenic regions is invariably low compared to splenules, it can be used as comparator for evaluating suspected splenic tissues.
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spelling pubmed-88714792022-02-25 Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis Holzgreve, Adrien Völter, Friederike Delker, Astrid Kunz, Wolfgang G. Fabritius, Matthias P. Brendel, Matthias Albert, Nathalie L. Bartenstein, Peter Unterrainer, Marcus Unterrainer, Lena M. Diagnostics (Basel) Article Background: Red blood cells (RBC) scintigraphy can be used not only for detection of bleeding sites, but also of spleen tissue. However, there is no established quantitative readout. Therefore, we investigated uptake in suspected splenic lesions in direct quantitative correlation to sites of physiologic uptake in order to objectify the readout. Methods: 20 patients with Tc-99m-labelled RBC scintigraphy and SPECT/low-dose CT for assessment of suspected splenic tissue were included. Lesions were rated as vital splenic or non-splenic tissue, and uptake and physiologic uptake of bone marrow, pancreas, and spleen were then quantified using a volume-of-interest based approach. Hepatic uptake served as a reference. Results: The median uptake ratio was significantly higher in splenic (2.82 (range, 0.58–24.10), n = 47) compared to other lesions (0.49 (0.01–0.83), n = 7), p < 0.001, and 5 lesions were newly discovered. The median pancreatic uptake was 0.09 (range 0.03–0.67), bone marrow 0.17 (0.03–0.45), and orthotopic spleen 14.45 (3.04–29.82). Compared to orthotopic spleens, the pancreas showed lowest uptake (0.09 vs. 14.45, p = 0.004). Based on pancreatic uptake we defined a cutoff (0.75) to distinguish splenic from other tissues. Conclusion: As the uptake in extra-splenic regions is invariably low compared to splenules, it can be used as comparator for evaluating suspected splenic tissues. MDPI 2022-02-14 /pmc/articles/PMC8871479/ /pubmed/35204576 http://dx.doi.org/10.3390/diagnostics12020486 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Holzgreve, Adrien
Völter, Friederike
Delker, Astrid
Kunz, Wolfgang G.
Fabritius, Matthias P.
Brendel, Matthias
Albert, Nathalie L.
Bartenstein, Peter
Unterrainer, Marcus
Unterrainer, Lena M.
Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis
title Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis
title_full Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis
title_fullStr Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis
title_full_unstemmed Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis
title_short Detection of Splenic Tissue Using (99m)Tc-Labelled Denatured Red Blood Cells Scintigraphy—A Quantitative Single Center Analysis
title_sort detection of splenic tissue using (99m)tc-labelled denatured red blood cells scintigraphy—a quantitative single center analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871479/
https://www.ncbi.nlm.nih.gov/pubmed/35204576
http://dx.doi.org/10.3390/diagnostics12020486
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