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FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports

Disclosure: R.S. Braham: None. C. Droumaguet: None. M. Vitellius: None. J. Tran-van-nhieu: None. E. Béquignon: None. P. Desgranges: None. N. Limal: None. M. Mahevas: None. B. Godeau: None. IgG4 thyroiditis is an invasive fibrotic process involving the thyroid in a systemic disease. It is a rare infl...

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Autores principales: Sarah Braham, Rim, Droumaguet, Céline, Vitellius, Manuel, Tran-van-nhieu, Jeanne, Béquignon, Emilie, Desgranges, Pascal, Limal, Nicolas, Mahevas, Matthieu, Godeau, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553696/
http://dx.doi.org/10.1210/jendso/bvad114.1876
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author Sarah Braham, Rim
Droumaguet, Céline
Vitellius, Manuel
Tran-van-nhieu, Jeanne
Béquignon, Emilie
Desgranges, Pascal
Limal, Nicolas
Mahevas, Matthieu
Godeau, Bertrand
author_facet Sarah Braham, Rim
Droumaguet, Céline
Vitellius, Manuel
Tran-van-nhieu, Jeanne
Béquignon, Emilie
Desgranges, Pascal
Limal, Nicolas
Mahevas, Matthieu
Godeau, Bertrand
author_sort Sarah Braham, Rim
collection PubMed
description Disclosure: R.S. Braham: None. C. Droumaguet: None. M. Vitellius: None. J. Tran-van-nhieu: None. E. Béquignon: None. P. Desgranges: None. N. Limal: None. M. Mahevas: None. B. Godeau: None. IgG4 thyroiditis is an invasive fibrotic process involving the thyroid in a systemic disease. It is a rare inflammatory autoimmune disease with insidious presentation and nonspecific symptoms.We describe two unusual cases of mass forming IgG4 thyroiditis that were diagnosed recently in our department. The first case is about a 42-year-old woman who has a history of Hashimoto thyroiditis with hypothyroidism presenting with a rapid goiter growth, neck pain, dysphagia and hoarseness. A lymphoma was suspected. Ultrasonography shows heterogeneous hypoechoic lesions that may infiltrate the perithyroid muscles. Fine-needle aspiration (FNA) was suspicious of IgG4 infiltrative disease which was confirmed by microbiopsy. Only the thyroid was hypermetabolic on fluorine-18 fluorodeoxyglucose (FDG) positron emission tomography (PET) Scan. No improvement under corticosteroid treatment and Rituximab. Surgery was planified to relieve pressure symptoms. The thyroid surgery was very difficult because of the extensive fibrosis and only a biopsy was performed, confirming the diagnosis and excluding malignancy. The second case is about a 68-year-old woman with a history of hypertension and Graves disease presented with a neck right mass that was suspected to be a paraganglioma, hypermetabolic on FDG PET scan with no other localisation. This mass was surrounding the right primitive carotid artery, associated with thrombi of the internal jugular vein. FNA and microbiopsy found a fibrotic non specific tissue. Thyroidectomy and surgical biopsy of the neck mass were performed with histopathology confirming IgG4 disease on the thyroid gland with fibrosis. There were no hypocalcemia in the two cases and no other localisation. IgG4 related mass-forming thyroiditis is an extremely rare disease. It is now a recognizable pattern of IgG4 thyroiditis, and has as differential diagnosis Hashimoto’s thyroiditis, Graves disease and thyroidal carcinoma.We will discuss through these cases the different clinical presentation of this rare disease, the diagnostic tools, the treatment and the long term follow up. Presentation: Friday, June 16, 2023
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spelling pubmed-105536962023-10-06 FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports Sarah Braham, Rim Droumaguet, Céline Vitellius, Manuel Tran-van-nhieu, Jeanne Béquignon, Emilie Desgranges, Pascal Limal, Nicolas Mahevas, Matthieu Godeau, Bertrand J Endocr Soc Thyroid Disclosure: R.S. Braham: None. C. Droumaguet: None. M. Vitellius: None. J. Tran-van-nhieu: None. E. Béquignon: None. P. Desgranges: None. N. Limal: None. M. Mahevas: None. B. Godeau: None. IgG4 thyroiditis is an invasive fibrotic process involving the thyroid in a systemic disease. It is a rare inflammatory autoimmune disease with insidious presentation and nonspecific symptoms.We describe two unusual cases of mass forming IgG4 thyroiditis that were diagnosed recently in our department. The first case is about a 42-year-old woman who has a history of Hashimoto thyroiditis with hypothyroidism presenting with a rapid goiter growth, neck pain, dysphagia and hoarseness. A lymphoma was suspected. Ultrasonography shows heterogeneous hypoechoic lesions that may infiltrate the perithyroid muscles. Fine-needle aspiration (FNA) was suspicious of IgG4 infiltrative disease which was confirmed by microbiopsy. Only the thyroid was hypermetabolic on fluorine-18 fluorodeoxyglucose (FDG) positron emission tomography (PET) Scan. No improvement under corticosteroid treatment and Rituximab. Surgery was planified to relieve pressure symptoms. The thyroid surgery was very difficult because of the extensive fibrosis and only a biopsy was performed, confirming the diagnosis and excluding malignancy. The second case is about a 68-year-old woman with a history of hypertension and Graves disease presented with a neck right mass that was suspected to be a paraganglioma, hypermetabolic on FDG PET scan with no other localisation. This mass was surrounding the right primitive carotid artery, associated with thrombi of the internal jugular vein. FNA and microbiopsy found a fibrotic non specific tissue. Thyroidectomy and surgical biopsy of the neck mass were performed with histopathology confirming IgG4 disease on the thyroid gland with fibrosis. There were no hypocalcemia in the two cases and no other localisation. IgG4 related mass-forming thyroiditis is an extremely rare disease. It is now a recognizable pattern of IgG4 thyroiditis, and has as differential diagnosis Hashimoto’s thyroiditis, Graves disease and thyroidal carcinoma.We will discuss through these cases the different clinical presentation of this rare disease, the diagnostic tools, the treatment and the long term follow up. Presentation: Friday, June 16, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10553696/ http://dx.doi.org/10.1210/jendso/bvad114.1876 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Thyroid
Sarah Braham, Rim
Droumaguet, Céline
Vitellius, Manuel
Tran-van-nhieu, Jeanne
Béquignon, Emilie
Desgranges, Pascal
Limal, Nicolas
Mahevas, Matthieu
Godeau, Bertrand
FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports
title FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports
title_full FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports
title_fullStr FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports
title_full_unstemmed FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports
title_short FRI531 IgG4 Related Mass -forming Thyroid Disease: Two Case Reports
title_sort fri531 igg4 related mass -forming thyroid disease: two case reports
topic Thyroid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553696/
http://dx.doi.org/10.1210/jendso/bvad114.1876
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