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Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex

BACKGROUND: Tuberous sclerosis complex (TSC) results in neurodevelopmental phenotypes, benign tumors, and cysts throughout the body. Recent studies show numerous rare findings in TSC. Guidelines suggest routine abdominal and chest imaging to monitor these thoracoabdominal findings, but imaging is no...

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Autores principales: Ritter, David M., Fessler, Bailey K., Ebrahimi-Fakhari, Daniel, Wei, Jun, Franz, David N., Krueger, Darcy A., Trout, Andrew T., Towbin, Alexander J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922878/
https://www.ncbi.nlm.nih.gov/pubmed/35292049
http://dx.doi.org/10.1186/s13023-022-02277-x
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author Ritter, David M.
Fessler, Bailey K.
Ebrahimi-Fakhari, Daniel
Wei, Jun
Franz, David N.
Krueger, Darcy A.
Trout, Andrew T.
Towbin, Alexander J.
author_facet Ritter, David M.
Fessler, Bailey K.
Ebrahimi-Fakhari, Daniel
Wei, Jun
Franz, David N.
Krueger, Darcy A.
Trout, Andrew T.
Towbin, Alexander J.
author_sort Ritter, David M.
collection PubMed
description BACKGROUND: Tuberous sclerosis complex (TSC) results in neurodevelopmental phenotypes, benign tumors, and cysts throughout the body. Recent studies show numerous rare findings in TSC. Guidelines suggest routine abdominal and chest imaging to monitor these thoracoabdominal findings, but imaging is not uniformly done across centers. Thus, the prevalence of many findings is unknown. To answer this, we categorized the clinical reads of 1398 thoracoabdominal scans from 649 patients of all ages in the Cincinnati Children’s Hospital TSC Repository Database. RESULTS: Typical TSC findings were present in many patients: kidney cysts (72%), kidney fat-containing angiomyolipomas (51%), kidney lipid-poor angiomyolipomas (27%), liver angiomyolipomas (19%), and lung nodules thought to represent multifocal micronodular pneumocyte hyperplasia (MMPH) (18%). While many features were more common in TSC2 patients, TSC1 patients had a higher prevalence of MMPH than TSC2 patients (24% versus 13%, p = 0.05). Many rare findings (e.g., lymphatic malformations and liver masses) are more common in TSC than in the general population. Additionally, most thoracoabdominal imaging findings increased with age except kidney cysts which decreased, with the 0–10 years age group having the highest percentage (69% 0–10 years, 49% 10–21 years, 48% 21 + years, p < 0.001). Finally, in our population, no patients had renal cell carcinoma found on abdominal imaging. CONCLUSIONS: These results show that regular thoracoabdominal scans in TSC may show several findings that should not be ignored or, conversely, over-reacted to when found in patients with TSC. Female sex, TSC2 mutation, and age are risk factors for many thoracoabdominal findings. The data suggest novel interactions of genetic mutation with pulmonary nodules and age with renal cysts. Finally, in agreement with other works, these findings indicate that several rare thoracoabdominal imaging findings occur at higher rates in the TSC population than in the general population. This work supports obtaining detailed thoracoabdominal imaging in patients with TSC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02277-x.
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spelling pubmed-89228782022-03-23 Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex Ritter, David M. Fessler, Bailey K. Ebrahimi-Fakhari, Daniel Wei, Jun Franz, David N. Krueger, Darcy A. Trout, Andrew T. Towbin, Alexander J. Orphanet J Rare Dis Research BACKGROUND: Tuberous sclerosis complex (TSC) results in neurodevelopmental phenotypes, benign tumors, and cysts throughout the body. Recent studies show numerous rare findings in TSC. Guidelines suggest routine abdominal and chest imaging to monitor these thoracoabdominal findings, but imaging is not uniformly done across centers. Thus, the prevalence of many findings is unknown. To answer this, we categorized the clinical reads of 1398 thoracoabdominal scans from 649 patients of all ages in the Cincinnati Children’s Hospital TSC Repository Database. RESULTS: Typical TSC findings were present in many patients: kidney cysts (72%), kidney fat-containing angiomyolipomas (51%), kidney lipid-poor angiomyolipomas (27%), liver angiomyolipomas (19%), and lung nodules thought to represent multifocal micronodular pneumocyte hyperplasia (MMPH) (18%). While many features were more common in TSC2 patients, TSC1 patients had a higher prevalence of MMPH than TSC2 patients (24% versus 13%, p = 0.05). Many rare findings (e.g., lymphatic malformations and liver masses) are more common in TSC than in the general population. Additionally, most thoracoabdominal imaging findings increased with age except kidney cysts which decreased, with the 0–10 years age group having the highest percentage (69% 0–10 years, 49% 10–21 years, 48% 21 + years, p < 0.001). Finally, in our population, no patients had renal cell carcinoma found on abdominal imaging. CONCLUSIONS: These results show that regular thoracoabdominal scans in TSC may show several findings that should not be ignored or, conversely, over-reacted to when found in patients with TSC. Female sex, TSC2 mutation, and age are risk factors for many thoracoabdominal findings. The data suggest novel interactions of genetic mutation with pulmonary nodules and age with renal cysts. Finally, in agreement with other works, these findings indicate that several rare thoracoabdominal imaging findings occur at higher rates in the TSC population than in the general population. This work supports obtaining detailed thoracoabdominal imaging in patients with TSC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02277-x. BioMed Central 2022-03-15 /pmc/articles/PMC8922878/ /pubmed/35292049 http://dx.doi.org/10.1186/s13023-022-02277-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ritter, David M.
Fessler, Bailey K.
Ebrahimi-Fakhari, Daniel
Wei, Jun
Franz, David N.
Krueger, Darcy A.
Trout, Andrew T.
Towbin, Alexander J.
Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
title Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
title_full Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
title_fullStr Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
title_full_unstemmed Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
title_short Prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
title_sort prevalence of thoracoabdominal imaging findings in tuberous sclerosis complex
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922878/
https://www.ncbi.nlm.nih.gov/pubmed/35292049
http://dx.doi.org/10.1186/s13023-022-02277-x
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