Riedel Thyroiditis

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Riedel Thyroiditis

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Riedel thyroiditis, or Riedel’s thyroiditis (RT), is a rare, chronic inflammatory disease of the thyroid gland characterized by a dense fibrosis that replaces normal thyroid parenchyma. The fibrotic process invades adjacent structures of the neck and extends beyond the thyroid capsule. This feature differentiates RT from other inflammatory or fibrotic disorders of the thyroid. Extension beyond the thyroid also differentiates this from the fibosing variant of Hashimoto thyroiditis. Gross pathology is shown in the image below. (See Etiology and Workup.)

Involvement in RT may be unilateral or bilobar. Thyroid function depends on the extent to which the normal thyroid gland has been replaced by fibrotic tissue. Most patients are euthyroid, but hypothyroidism is noted in approximately 30% of cases. Rarely, hyperthyroidism can occur, but this is probably secondary to a coexisting condition. (See Prognosis, Presentation, and Workup.)

Some experts have traditionally believed that RT is not primarily a thyroid disease but rather that it is a manifestation of the systemic disorder multifocal fibrosclerosis. Approximately one third of RT cases are associated with clinical findings of multifocal fibrosclerosis at the time of diagnosis. (See Etiology.)

In 1883, Professor Bernhard Riedel first recognized the disease. He published a description of 2 cases in 1896 and of a third case in 1897. [1] Riedel used the term eisenharte struma to describe the stone-hard consistency of the thyroid gland and its fixation to adjacent structures. He noted the presence of chronic inflammation with fibrosis and the absence of malignancy on microscopic examination. Simple wedge resection of the thyroid isthmus was used to alleviate tracheal obstruction and is still the preferred surgical therapy for RT.

Because of the encroachment beyond the thyroid capsule, nonthyroid problems can be associated with RT. Complications of Riedel thyroiditis can include the following:

Airway obstruction

Dysphonia

Hoarseness – Due to recurrent laryngeal involvement

Hypothyroidism

Hypoparathyroidism

Dysphagia

Stridor – Due to tracheal compression

The etiology of Riedel thyroiditis (RT) is unknown, but it may be related to a relatively new group of rare disorders, IgG4-related systemic disease (IgG4-RSD). [2] One theory of pathogenesis postulates that RT results from an autoimmune process. A second theory holds RT to be a primary fibrotic disorder. However, IgG4-RSD may unify these 2 seemingly disparate etiologies.

The following evidence supports an autoimmune pathogenesis for RT:

The presence of antithyroid antibodies in a significant percentage of patients with RT (67% of 178 cases reviewed in one study) [3]

The pathologic features of cellular infiltration, including lymphocytes, plasma cells, and histiocytes

The frequent presence of focal vasculitis on pathologic examination

The favorable response of a subset of patients with RT to treatment with systemic corticosteroids

However, the presence of normal lymphocyte subpopulations and normal serum complement levels weighs against an autoimmune mechanism. Elevated levels of antithyroid antibodies may merely reflect the immune system’s exposure to sequestered antigens released by the destruction of thyroid parenchyma from a primary fibrotic disorder.

The theory that RT is a primary fibrotic disorder is supported by its association with multifocal fibrosclerosis. This uncommon idiopathic syndrome is characterized by fibrosis involving multiple organ systems. The extracervical manifestations of multifocal fibrosclerosis can include retroperitoneal fibrosis, mediastinal fibrosis, orbital pseudotumor, pulmonary fibrosis, sclerosing cholangitis, lacrimal gland fibrosis, and fibrous parotitis. RT may be but 1 manifestation of this multifocal disease.

The histopathologic changes of RT closely resemble those observed in multifocal fibrosclerosis. Additionally, one third of published RT cases have demonstrated at least 1 manifestation of extracervical fibrosclerosis. The ability of systemic corticosteroids and tamoxifen to inhibit fibrogenesis accounts for the favorable effect of such treatment in both conditions. [4]

IgG4-RSD is a relatively new group of disorders that share similar presentations. These disorders have in common a preponderance of excess IgG4. The disorders are characterized by lymphoplasmacytic infiltrates containing IgG4-positive plasma cells. [5] These infiltrates ultimately lead to fibrosis and elevated serum levels of IgG4. [6, 7]

Riedel thyroiditis (RT) is a very rare condition. At the Mayo Clinic, 37 cases of RT were diagnosed in a series of 57,000 thyroidectomies performed between 1920 and 1984, for an incidence of 0.06%. The overall incidence among outpatients was 1.6 cases per 100,000 population. Based on large databases in referral centers, it appears that over the previous decades, the incidence of RT has been decreasing.

Although predominantly reported in whites, RT has been described in all races. RT is most often seen in women; in a review of 178 patients with RT, 83% were female. In the same study, the mean age at diagnosis of RT was 47.8 years (range, 23-77 y). [3]

Riedel thyroiditis (RT) is generally a self-limited disease with a favorable prognosis. Death due to airway compromise is very rare in treated patients. Occasionally, spontaneous remission has been reported. Patients can also relapse.

In RT, morbidity is most frequently related to local compressive symptoms, such as dysphagia, dyspnea, hoarseness, and cough. Hypothyroidism is present in 30% of cases. Fibrotic invasion of adjacent anatomic structures may infrequently result in symptoms related to recurrent laryngeal nerve paralysis or hypoparathyroidism.

One third of patients with RT ultimately develop at least 1 extracervical manifestation of multifocal fibrosclerosis (such as retroperitoneal fibrosis, mediastinal fibrosis, or sclerosing cholangitis). [8] In such patients, the prognosis essentially becomes that of extracervical fibrosclerosis. Therefore, when RT is diagnosed, it is essential to perform abdominal and chest imaging studies to exclude concomitant, extracervical entities from multifocal fibrosclerosis. Fibrosclerosis of the surrounding tissue by RT can lead to serious morbidity and death.

A retrospective institutional review of a rare form of invasive thyroiditis from the Mayo Clinic discussed the common presenting symptoms and extrathyroidal involvement of the systemic fibrosclerosis. Treatments used in the 21 reported patients included partial thyroidectomy, tamoxifen, and corticosteroid therapy. Other, less well validated studies include mycophenolate mofetil [9] and rituximab. [10] Of note, no cause-specific mortality was noted, and the fibrotic process stabilized or partially resolved in all patients. [4]

Riedel BM. Die chronische, zur Bildung eisenharter Tumoren fuhrende Entzundung der Schilddruse. Verh Dtsch Ges Chir. 1896. 25:101-5.

Katabathina VS, Khalil S, Shin S, Lath N, Menias CO, Prasad SR. Immunoglobulin G4-Related Disease: Recent Advances in Pathogenesis and Imaging Findings. Radiol Clin North Am. 2016 May. 54 (3):535-51. [Medline].

Schwaegerle SM, Bauer TW, Esselstyn CB Jr. Riedel’s thyroiditis. Am J Clin Pathol. 1988 Dec. 90(6):715-22. [Medline].

Fatourechi MM, Hay ID, McIver B, Sebo TJ, Fatourechi V. Invasive fibrous thyroiditis (riedel thyroiditis): the mayo clinic experience, 1976-2008. Thyroid. 2011 Jul. 21(7):765-72. [Medline].

Pusztaszeri M, Triponez F, Pache JC, Bongiovanni M. Riedel’s thyroiditis with increased IgG4 plasma cells: evidence for an underlying IgG4-related sclerosing disease?. Thyroid. 2012 Sep. 22(9):964-8. [Medline].

Divatia M, Kim SA, Ro JY. IgG4-related sclerosing disease, an emerging entity: a review of a multi-system disease. Yonsei Med J. 2012 Jan. 53(1):15-34. [Medline]. [Full Text].

Dahlgren M, Khosroshahi A, Nielsen GP, Deshpande V, Stone JH. Riedel’s thyroiditis and multifocal fibrosclerosis are part of the IgG4-related systemic disease spectrum. Arthritis Care Res (Hoboken). 2010 Sep. 62(9):1312-8. [Medline].

Oguz KK, Kiratli H, Oguz O, et al. Multifocal fibrosclerosis: a new case report and review of the literature. Eur Radiol. 2002 May. 12(5):1134-8. [Medline].

Levy JM, Hasney CP, Friedlander PL, Kandil E, Occhipinti EA, Kahn MJ. Combined mycophenolate mofetil and prednisone therapy in tamoxifen- and prednisone-resistant Reidel’s thyroiditis. Thyroid. 2010 Jan. 20(1):105-7. [Medline].

Soh SB, Pham A, O’Hehir RE, Cherk M, Topliss DJ. Novel use of rituximab in a case of Riedel’s thyroiditis refractory to glucocorticoids and tamoxifen. J Clin Endocrinol Metab. 2013 Sep. 98(9):3543-9. [Medline].

Hennessey JV. Clinical review: Riedel’s thyroiditis: a clinical review. J Clin Endocrinol Metab. 2011 Oct. 96(10):3031-41. [Medline].

Perimenis P, Marcelli S, Leteurtre E, et al. [Riedel’s thyroiditis: current aspects]. Presse Med. 2008 Jun. 37(6 Pt 2):1015-21. [Medline].

Li Y, Nishihara E, Kakudo K. Hashimoto’s thyroiditis: old concepts and new insights. Curr Opin Rheumatol. 2011 Jan. 23(1):102-7. [Medline].

Morselli-Labate AM, Pezzilli R. Usefulness of serum IgG4 in the diagnosis and follow up of autoimmune pancreatitis: A systematic literature review and meta-analysis. J Gastroenterol Hepatol. 2009 Jan. 24(1):15-36. [Medline].

Khosroshahi A, Stone JR, Pratt DS, Deshpande V, Stone JH. Painless jaundice with serial multi-organ dysfunction. Lancet. 2009 Apr 25. 373(9673):1494. [Medline].

Drieskens O, Blockmans D, Van den Bruel A, et al. Riedel’s thyroiditis and retroperitoneal fibrosis in multifocal fibrosclerosis: positron emission tomographic findings. Clin Nucl Med. 2002 Jun. 27(6):413-5. [Medline].

Kotilainen P, Airas L, Kojo T, et al. Positron emission tomography as an aid in the diagnosis and follow-up of Riedel’s thyroiditis. Eur J Intern Med. 2004. 15:186-9.

Beahrs OH, McConahey WM, Woolner LB. Invasive fibrous thyroiditis (Riedel’s struma). J Clin Endocrinol Metab. 1957 Feb. 17(2):201-20. [Medline].

Lorenz K, Gimm O, Holzhausen HJ, et al. Riedel’s thyroiditis: impact and strategy of a challenging surgery. Langenbecks Arch Surg. 2007 Jul. 392(4):405-12. [Medline].

Lo JC, Loh KC, Rubin AL, et al. Riedel’s thyroiditis presenting with hypothyroidism and hypoparathyroidism: dramatic response to glucocorticoid and thyroxine therapy. Clin Endocrinol (Oxf). 1998 Jun. 48(6):815-8. [Medline].

Vaidya B, Harris PE, Barrett P, et al. Corticosteroid therapy in Riedel’s thyroiditis. Postgrad Med J. 1997 Dec. 73(866):817-9. [Medline].

Few J, Thompson NW, Angelos P, et al. Riedel’s thyroiditis: treatment with tamoxifen. Surgery. 1996 Dec. 120(6):993-8; discussion 998-9. [Medline].

De M, Jaap A, Dempster J. Tamoxifen therapy in steroid resistant Reidel’s thyroiditis. Scott Med J. 2001 Apr. 46(2):56-7. [Medline].

Jung YJ, Schaub CR, Rhoades R, et al. A case of Riedel’s thyroiditis treated with tamoxifen: another successful outcome. Endocr Pract. 2004. 10(6):483-6.

Pritchyk K, Newkirk K, Garlich P, et al. Tamoxifen therapy for Riedel’s thyroiditis. Laryngoscope. 2004 Oct. 114(10):1758-60. [Medline].

Levy JM, Hasney CP, Friedlander PL, Kandil E, Occhipinti EA, Kahn MJ. Combined mycophenolate mofetil and prednisone therapy in tamoxifen- and prednisone-resistant Reidel’s thyroiditis. Thyroid. 2010 Jan. 20(1):105-7. [Medline].

Khosroshahi A, Stone JH. A clinical overview of IgG4-related systemic disease. Curr Opin Rheumatol. 2011 Jan. 23(1):57-66. [Medline].

Chris K Guerin, MD, FACE Director, Diabetes Education Services, Chief, Division of Endocrinology, Tri-City Medical Center; Assistant Clinical Professor of Medicine, University of California, San Diego, School of Medicine

Chris K Guerin, MD, FACE is a member of the following medical societies: American Association of Clinical Endocrinologists, American Diabetes Association, National Lipid Association

Disclosure: Nothing to disclose.

George T Griffing, MD Professor Emeritus of Medicine, St Louis University School of Medicine

George T Griffing, MD is a member of the following medical societies: American Association for the Advancement of Science, International Society for Clinical Densitometry, Southern Society for Clinical Investigation, American College of Medical Practice Executives, American Association for Physician Leadership, American College of Physicians, American Diabetes Association, American Federation for Medical Research, American Heart Association, Central Society for Clinical and Translational Research, Endocrine Society

Disclosure: Nothing to disclose.

John Boone, MD Consulting Staff, Department of Otolaryngology, Naval Hospital Oak Harbor

John Boone, MD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery

Disclosure: Nothing to disclose.

Stephanie L Lee, MD, PhD Associate Professor, Department of Medicine, Boston University School of Medicine; Director of Thyroid Health Center, Associate Chief, Section of Endocrinology, Diabetes and Nutrition, Boston Medical Center; Fellow, Association of Clinical Endocrinology

Stephanie L Lee, MD, PhD is a member of the following medical societies: American College of Endocrinology, American Thyroid Association, and Endocrine Society

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Kent Wehmeier, MD Professor, Department of Internal Medicine, Division of Endocrinology, Diabetes, and Metabolism, St Louis University School of Medicine

Kent Wehmeier, MD is a member of the following medical societies: American Society of Hypertension, Endocrine Society, and International Society for Clinical Densitometry

Disclosure: Nothing to disclose.

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