Author, year
Number of patients
Type of study
Main results
Li et al. (2010) [8]
70
Histological case-control study of IgG4-thyroiditis and non-IgG4 thyroiditis
IgG4-thyroiditis and non-IgG4 thyroiditis are distinct entities
Li et al. (2009) [12]
17
Histological cohort study
Immunostaining of IgG4 can help subclassify HT
Ceresini et al. (2015) [16]
144
Prospective ultrasonographic and laboratory case-control study
Patients with idiopathic retroperitoneal fibrosis have a higher risk of HT compared to controls
Dahlgren et al. (2010) [20]
3
Retrospective histological study
Riedel’s thyroiditis is part of the IgG4-related systemic diseases
Watanabe et al. (2013) [23]
114
Retrospective study in patients with IgG-4-related disease
Serum IgG4 are higher in hypothyroid subjects
Li et al. (2012) [24]
105 cases of HT
Retrospective histological study
In IgG4 HT histopathological features are distinct from non-IgG4 HT
Kawashima et al. (2014) [26]
24 HT patients with elevated serum IgG
Measure of serum IgG-4 in a prospective study
Serum IgG-4 elevated in five patients
Zhang et al. (2014) [25]
53 cases of HT patients
Histological and laboratory cohort study
HT can be divided into IgG4-positive and IgG4-negative
7.9 Imaging
Sonographic studies have revealed that IgG4-thyroiditis is significantly associated with diffuse low echogenicity, whereas non-IgG4 thyroiditis seems to be associated with diffuse coarse echogenicity.
Several sonographic patterns have been reported in HT [33–35] and studies aimed at the identification of an association between sonographic findings and the degree of thyroid function impairment have been conducted [36, 37]. Data have been reported demonstrating that patients with remarkable hypoechogenicity of the thyroid gland (i.e., the echogenicity of the thyroid was almost equal to or less than that of the adjacent muscles) had abnormally low T4 and abnormally high TSH more frequently than patients with coarse echogenicity. Thus, the observation that IgG4-thyroiditis is significantly associated with diffuse low echogenicity is likely to suggest that this form is more frequently associated with hypothyroidism and follicular degeneration [2]. See Fig. 7.1 for representative ultrasound images of normal thyroid and chronic Hashimoto’s thyroiditis.
Fig. 7.1
Representative ultrasound images of normal thyroid (a) with homogeneous texture, and chronic autoimmune (Hashimoto’s) thyroiditis (b) characterized by hypoechogenicity and inhomogeneous texture
7.10 Future Perspectives and Hypothesis of Treatment
The potential association between IgG4-RD and thyroid disease represents a matter of increasing interest. There is no doubt that larger studies are needed in order to better define this relationship. Identifying subsets of patients with IgG4-thyroiditis, based either on tissue or serum findings, could be important for several clinical aspects. The more rapid progression towards surgery due to thyroid gland enlargement in the IgG4-thyroiditis subgroup could lead investigators to explore whether this subset warrants immunosuppressive therapy, and whether immunosuppression may halt disease progression. In addition, a more rapid loss of thyroid function of IgG4-thyroiditis patients may lead to earlier interventions in treating hypothyroidism. Finally, from an investigative perspective, IgG4-related and -unrelated forms of thyroiditis may recognize different proteins as target antigens of autoantibody production, and may reveal different immunopathogenic patterns leading to thyroid inflammation and fibrosis.
References
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Sato Y et al (2010) IgG4-related disease: historical overview and pathology of hematological disorders. Pathol Int 60:247–258CrossRefPubMed