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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7669956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
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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