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A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma

BACKGROUND: Marine Lenhart syndrome is a rare disease and causes refractory hyperthyroidism. So far, little evidence on the combination of both Marine Lenhart syndrome and Hashimoto's thyroiditis is available. We suspect that Marine Lenhart syndrome when combined with Hashimoto's thyroidit...

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Autores principales: Ye, Peng, Li, Lan, Wei, Dong, Li, Fan, Zhong, Yuan, Zeng, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463925/
https://www.ncbi.nlm.nih.gov/pubmed/37641098
http://dx.doi.org/10.1186/s12902-023-01438-8
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author Ye, Peng
Li, Lan
Wei, Dong
Li, Fan
Zhong, Yuan
Zeng, Jing
author_facet Ye, Peng
Li, Lan
Wei, Dong
Li, Fan
Zhong, Yuan
Zeng, Jing
author_sort Ye, Peng
collection PubMed
description BACKGROUND: Marine Lenhart syndrome is a rare disease and causes refractory hyperthyroidism. So far, little evidence on the combination of both Marine Lenhart syndrome and Hashimoto's thyroiditis is available. We suspect that Marine Lenhart syndrome when combined with Hashimoto's thyroiditis might have its particular features, which are not exactly the same as those of the isolated Marine Lenhart syndrome. CASE PRESENTATION: A 56-year-old middle-aged man presented with recurrent hyperthyroidism, and Graves' disease combined with Hashimoto's thyroiditis was considered. Radionuclide imaging showed a hot nodule, but ultrasonography suggested the possibility of malignancy with a category of 4B according to the Chinese-Thyroid Imaging-Reporting and Data System (C-TIRADS) model. Fine needle aspiration cytology (FNAC) revealed eosinophilic follicular lesions with papillary features, and prompted that papillary thyroid carcinoma could not be excluded. Partial thyroidectomy was performed and the nodule was proven to be benign by histopathology. The final diagnosis was atypical Marine Lenhart syndrome with Hashimoto's thyroiditis. CONCLUSIONS: Marine Lenhart syndrome combined with Hashimoto's thyroiditis has its particular characteristics, showing some signs mimicking malignancy. Limitations of ultrasonography and FNAC in diagnosis should be noted in these scenarios.
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spelling pubmed-104639252023-08-30 A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma Ye, Peng Li, Lan Wei, Dong Li, Fan Zhong, Yuan Zeng, Jing BMC Endocr Disord Case Report BACKGROUND: Marine Lenhart syndrome is a rare disease and causes refractory hyperthyroidism. So far, little evidence on the combination of both Marine Lenhart syndrome and Hashimoto's thyroiditis is available. We suspect that Marine Lenhart syndrome when combined with Hashimoto's thyroiditis might have its particular features, which are not exactly the same as those of the isolated Marine Lenhart syndrome. CASE PRESENTATION: A 56-year-old middle-aged man presented with recurrent hyperthyroidism, and Graves' disease combined with Hashimoto's thyroiditis was considered. Radionuclide imaging showed a hot nodule, but ultrasonography suggested the possibility of malignancy with a category of 4B according to the Chinese-Thyroid Imaging-Reporting and Data System (C-TIRADS) model. Fine needle aspiration cytology (FNAC) revealed eosinophilic follicular lesions with papillary features, and prompted that papillary thyroid carcinoma could not be excluded. Partial thyroidectomy was performed and the nodule was proven to be benign by histopathology. The final diagnosis was atypical Marine Lenhart syndrome with Hashimoto's thyroiditis. CONCLUSIONS: Marine Lenhart syndrome combined with Hashimoto's thyroiditis has its particular characteristics, showing some signs mimicking malignancy. Limitations of ultrasonography and FNAC in diagnosis should be noted in these scenarios. BioMed Central 2023-08-28 /pmc/articles/PMC10463925/ /pubmed/37641098 http://dx.doi.org/10.1186/s12902-023-01438-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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 Case Report
Ye, Peng
Li, Lan
Wei, Dong
Li, Fan
Zhong, Yuan
Zeng, Jing
A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma
title A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma
title_full A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma
title_fullStr A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma
title_full_unstemmed A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma
title_short A case of Marine Lenhart syndrome with Hashimoto’s thyroiditis that mimicked thyroid carcinoma
title_sort case of marine lenhart syndrome with hashimoto’s thyroiditis that mimicked thyroid carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463925/
https://www.ncbi.nlm.nih.gov/pubmed/37641098
http://dx.doi.org/10.1186/s12902-023-01438-8
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