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IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report

Patient: Female, 69-year-old Final Diagnosis: Riedel thyroiditis Symptoms: Dysphagia • goiter Medication: — Clinical Procedure: — Specialty: Endocrinology and Metabolic OBJECTIVE: Rare disease BACKGROUND: Riedel’s thyroiditis is a rare form of immunoglobulin G (IgG) 4-related invasive fibrosis of th...

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Autores principales: Navarro-Sánchez, Valeria, Marín-Castañeda, Luis Antonio, Gallegos, Cecilia A., Quiroz, Oscar, Ahumada-Ayala, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669956/
https://www.ncbi.nlm.nih.gov/pubmed/33177482
http://dx.doi.org/10.12659/AJCR.928046
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author Navarro-Sánchez, Valeria
Marín-Castañeda, Luis Antonio
Gallegos, Cecilia A.
Quiroz, Oscar
Ahumada-Ayala, Miguel
author_facet Navarro-Sánchez, Valeria
Marín-Castañeda, Luis Antonio
Gallegos, Cecilia A.
Quiroz, Oscar
Ahumada-Ayala, Miguel
author_sort Navarro-Sánchez, Valeria
collection PubMed
description Patient: Female, 69-year-old Final Diagnosis: Riedel thyroiditis Symptoms: Dysphagia • goiter Medication: — Clinical Procedure: — Specialty: Endocrinology and Metabolic OBJECTIVE: Rare disease BACKGROUND: Riedel’s thyroiditis is a rare form of immunoglobulin G (IgG) 4-related invasive fibrosis of the thyroid gland; given its scarce incidence, standardized therapeutic guidelines are unavailable. Although complications are unusual, obstructive symptoms produced by the stony-hard goiter may put patients’ lives at risk. The diagnosis must be biopsy-proven, and treatment consists of thyroid hormone replacement and anti-inflammatory drugs, although sometimes thyroidectomy may be required. CASE REPORT: A 69-year-old woman presented with a 7-month history of progressive hypothyroidism and obstructive dysphagia. On physical examination, she had a large, stony-hard goiter. A Doppler ultrasound study revealed a massive, avascular enlargement of the thyroid gland. A computed tomography scan failed to demonstrate any extrathyroidal extension of the abnormal tissue. A Tru-Cut biopsy of the thyroid was performed. Extensive replacement of thyroid follicles by prominent bands of fibrous tissue was observed, with follicular obliteration and mild focal occlusive phlebitis. A lymphoplasmacytic infiltrate was clearly identified; no oxyphilic nor giant cells were found. On immunohistochemistry, the immunoglobulin G (IgG) 4/IgG ratio in the plasma cell infiltrate was 40%; increased serum IgG4 levels were also found, supporting the diagnosis of Riedel’s thyroiditis. The patient was successfully treated with levothyroxine replacement and tamoxifen with prompt resolution of obstructive symptoms. CONCLUSIONS: Fibrous thyroiditis should be considered in the differential diagnosis of primary hypothyroidism in a patient with a stony-hard goiter. Although steroids are often used as a therapeutic strategy for this disease, our patient had an excellent therapeutic response to tamoxifen, avoiding adverse effects associated with steroid therapy, the higher cost of monoclonal antibody therapy, and surgery-associated risks.
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spelling pubmed-76699562020-11-23 IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report Navarro-Sánchez, Valeria Marín-Castañeda, Luis Antonio Gallegos, Cecilia A. Quiroz, Oscar Ahumada-Ayala, Miguel Am J Case Rep Articles Patient: Female, 69-year-old Final Diagnosis: Riedel thyroiditis Symptoms: Dysphagia • goiter Medication: — Clinical Procedure: — Specialty: Endocrinology and Metabolic OBJECTIVE: Rare disease BACKGROUND: Riedel’s thyroiditis is a rare form of immunoglobulin G (IgG) 4-related invasive fibrosis of the thyroid gland; given its scarce incidence, standardized therapeutic guidelines are unavailable. Although complications are unusual, obstructive symptoms produced by the stony-hard goiter may put patients’ lives at risk. The diagnosis must be biopsy-proven, and treatment consists of thyroid hormone replacement and anti-inflammatory drugs, although sometimes thyroidectomy may be required. CASE REPORT: A 69-year-old woman presented with a 7-month history of progressive hypothyroidism and obstructive dysphagia. On physical examination, she had a large, stony-hard goiter. A Doppler ultrasound study revealed a massive, avascular enlargement of the thyroid gland. A computed tomography scan failed to demonstrate any extrathyroidal extension of the abnormal tissue. A Tru-Cut biopsy of the thyroid was performed. Extensive replacement of thyroid follicles by prominent bands of fibrous tissue was observed, with follicular obliteration and mild focal occlusive phlebitis. A lymphoplasmacytic infiltrate was clearly identified; no oxyphilic nor giant cells were found. On immunohistochemistry, the immunoglobulin G (IgG) 4/IgG ratio in the plasma cell infiltrate was 40%; increased serum IgG4 levels were also found, supporting the diagnosis of Riedel’s thyroiditis. The patient was successfully treated with levothyroxine replacement and tamoxifen with prompt resolution of obstructive symptoms. CONCLUSIONS: Fibrous thyroiditis should be considered in the differential diagnosis of primary hypothyroidism in a patient with a stony-hard goiter. Although steroids are often used as a therapeutic strategy for this disease, our patient had an excellent therapeutic response to tamoxifen, avoiding adverse effects associated with steroid therapy, the higher cost of monoclonal antibody therapy, and surgery-associated risks. International Scientific Literature, Inc. 2020-11-12 /pmc/articles/PMC7669956/ /pubmed/33177482 http://dx.doi.org/10.12659/AJCR.928046 Text en © Am J Case Rep, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Navarro-Sánchez, Valeria
Marín-Castañeda, Luis Antonio
Gallegos, Cecilia A.
Quiroz, Oscar
Ahumada-Ayala, Miguel
IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report
title IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report
title_full IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report
title_fullStr IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report
title_full_unstemmed IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report
title_short IgG4-Related Fibrous Thyroiditis (Riedel’s Thyroiditis): A Case Report
title_sort igg4-related fibrous thyroiditis (riedel’s thyroiditis): a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669956/
https://www.ncbi.nlm.nih.gov/pubmed/33177482
http://dx.doi.org/10.12659/AJCR.928046
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