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Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex

Tuberous-sclerosis-complex (TSC) is associated with a high lifetime risk of severe complications. Clinical manifestations are largely variable and diagnosis is often missed. Sclerotic-bone-lesions (SBL) could represent a potential imaging biomarker for the diagnosis of TSC. In this study, computed t...

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Autores principales: Brakemeier, Susanne, Vogt, Lars, Adams, Lisa C., Zukunft, Bianca, Diederichs, Gerd, Hamm, Bernd, Budde, Klemens, Eckardt, Kai-Uwe, Makowski, Marcus R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772483/
https://www.ncbi.nlm.nih.gov/pubmed/29343816
http://dx.doi.org/10.1038/s41598-018-19399-7
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author Brakemeier, Susanne
Vogt, Lars
Adams, Lisa C.
Zukunft, Bianca
Diederichs, Gerd
Hamm, Bernd
Budde, Klemens
Eckardt, Kai-Uwe
Makowski, Marcus R.
author_facet Brakemeier, Susanne
Vogt, Lars
Adams, Lisa C.
Zukunft, Bianca
Diederichs, Gerd
Hamm, Bernd
Budde, Klemens
Eckardt, Kai-Uwe
Makowski, Marcus R.
author_sort Brakemeier, Susanne
collection PubMed
description Tuberous-sclerosis-complex (TSC) is associated with a high lifetime risk of severe complications. Clinical manifestations are largely variable and diagnosis is often missed. Sclerotic-bone-lesions (SBL) could represent a potential imaging biomarker for the diagnosis of TSC. In this study, computed tomography (CT) data sets of 49 TSC patients (31 females) were included and compared to an age/sex matched control group. Imaging features of SBLs included frequency, size and location pattern. Sensitivities, specificities and cutoff values for the diagnosis of TSC were established for the skull, thorax, and abdomen/pelvis. In TSC patients, 3439 SBLs were detected, including 665 skull SBLs, 1426 thoracal SBLs and 1348 abdominal/pelvic SBLs. In the matched control-collective, 157 SBLs could be found. The frequency of SBLs enabled a reliable differentiation between TSC patients and the control collective with the following sensitivities and specificities. Skull: ≥5 SBLs, 0.783, 1; thorax: ≥4 SBLs, 0.967, 0.967; abdomen/pelvis: ≥5 SBLs: 0.938, 0.906. SBL size was significantly larger compared to controls (p < 0.05). Based on the frequency, size and location pattern of SBLs TSC can be suspected. SBLs may serve as a potential imaging biomarker in the workup of TSC patients.
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spelling pubmed-57724832018-01-26 Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex Brakemeier, Susanne Vogt, Lars Adams, Lisa C. Zukunft, Bianca Diederichs, Gerd Hamm, Bernd Budde, Klemens Eckardt, Kai-Uwe Makowski, Marcus R. Sci Rep Article Tuberous-sclerosis-complex (TSC) is associated with a high lifetime risk of severe complications. Clinical manifestations are largely variable and diagnosis is often missed. Sclerotic-bone-lesions (SBL) could represent a potential imaging biomarker for the diagnosis of TSC. In this study, computed tomography (CT) data sets of 49 TSC patients (31 females) were included and compared to an age/sex matched control group. Imaging features of SBLs included frequency, size and location pattern. Sensitivities, specificities and cutoff values for the diagnosis of TSC were established for the skull, thorax, and abdomen/pelvis. In TSC patients, 3439 SBLs were detected, including 665 skull SBLs, 1426 thoracal SBLs and 1348 abdominal/pelvic SBLs. In the matched control-collective, 157 SBLs could be found. The frequency of SBLs enabled a reliable differentiation between TSC patients and the control collective with the following sensitivities and specificities. Skull: ≥5 SBLs, 0.783, 1; thorax: ≥4 SBLs, 0.967, 0.967; abdomen/pelvis: ≥5 SBLs: 0.938, 0.906. SBL size was significantly larger compared to controls (p < 0.05). Based on the frequency, size and location pattern of SBLs TSC can be suspected. SBLs may serve as a potential imaging biomarker in the workup of TSC patients. Nature Publishing Group UK 2018-01-17 /pmc/articles/PMC5772483/ /pubmed/29343816 http://dx.doi.org/10.1038/s41598-018-19399-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Brakemeier, Susanne
Vogt, Lars
Adams, Lisa C.
Zukunft, Bianca
Diederichs, Gerd
Hamm, Bernd
Budde, Klemens
Eckardt, Kai-Uwe
Makowski, Marcus R.
Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
title Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
title_full Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
title_fullStr Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
title_full_unstemmed Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
title_short Sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
title_sort sclerotic bone lesions as a potential imaging biomarker for the diagnosis of tuberous sclerosis complex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772483/
https://www.ncbi.nlm.nih.gov/pubmed/29343816
http://dx.doi.org/10.1038/s41598-018-19399-7
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