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Subacute thyroiditis during early pregnancy: a case report and literature review

A Correction to this article was published on 31 January 2022

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Abstract

Background

Subacute thyroiditis (SAT) is rarely diagnosed in pregnant women, and only 7 cases have been reported to date. Thyroid dysfunction, especially hyperthyroidism, during pregnancy has been associated with both maternal and neonatal complications. Thus, the early diagnosis and treatment of SAT during pregnancy may be beneficial. We present a case report and literature review to complement the diagnostic evaluation and management of SAT during pregnancy.

Case presentation

A 27-year-old woman presented in gestational week 17 of her first pregnancy and had a negative prior medical history. She presented to the Endocrinology Department complaining of neck pain for one month that had intensified in the last five days. Physical examination revealed a diffusely enlarged thyroid gland that was firm and tender on palpation. The patient also had an elevated temperature and heart rate. The increasing and long-lasting pain coupled with a decreased level of thyroid-stimulating hormone indicated hyperthyroidism. Ultrasound findings were indicative of SAT. Importantly, the pain was so severe that 10 mg of oral prednisone per day was administered in gestational week 18, which was increased to 15 mg/d after 10 days that was discontinued in week 28. Levothyroxine was started in gestational week 24 and administered throughout the pregnancy. The patient responded well to the treatments, and her neck pain disappeared in gestational week 21. She gave birth to a healthy male in gestational week 41.

Conclusion

SAT can be diagnosed and effectively managed during pregnancy, thus benefiting mothers and infants.

Peer Review reports

Background

The incidence of maternal thyroid disorders remains high during pregnancy, with hypothyroidism affecting up to 2%—3% of all pregnancies and hyperthyroidism affecting 0.1%—0.4%. Subacute thyroiditis (SAT) accounts for 5% of patients with thyroid disease [1], Pregnant women with clinical and subclinical hypothyroidism increased the risk of preterm delivery by 4.4 times—3.0 times respectively. Clinical hyperthyroidism is also significantly associated with fetal distress [2]. SAT is also called granulomatous thyroiditis or giant cell thyroiditis, and is regarded as a self-limiting inflammatory disorder.

The majority of SAT patients are women between the ages of 30 and 50 years. SAT is secondary to virus infection and is frequently accompanied by neck pain, fever, fatigue, and myalgia, followed by diffuse enlargement and tenderness of the thyroid gland [3, 4]. Laboratory examination tends to show an increase in the level of erythrocyte sedimentation rate (ESR), white blood cell count, C-reactive protein (CRP), and other indicators of infection, coupled with the low echogenicity of nodules on ultrasound and decreased iodine absorption rate. SAT in pregnancy is extremely rare and is frequently misdiagnosed as hyperthyroidism. While 25% of patients have hyperthyroidism in pregnancy [5], hyperthyroidism caused by SAT during pregnancy is uncommon, with only 7 cases reported to date [5,6,7,8,9,10].

Herein, we present a case of SAT diagnosed in the first trimester of pregnancy in the Endocrinology Department of the Second People’s Hospital of Yunnan Province (Yunnan, China).

Case presentation

A 27-year-old women in the 17th week of gestation in her first pregnancy presented to the Endocrinology Department of our hospital complaining of neck pain for one month that had intensified in the last five days. The neck pain appeared at the 12th week of gestation, which was on the left side without any obvious cause and radiated to the jaw. It was initially tolerable, and there were no other symptoms, such as chills, fever, palpitations, tremor, or sweating. The pain gradually shifted to the right side and the patient requested no medication for her discomfort. In the 17th week of gestation, the patient suffered from severe neck pain, which seriously affected quality of life and sleep and she expressed a strong willingness to undergo treatment.

The patient had throat pain for 3 days before pregnancy, which improved without treatment and had no personal or family history of thyroid disease. Her menstrual cycle was regular before pregnancy. She had an axillary temperature of 37.4 °C, increased resting heart rate of 98 beats/min, and normal blood pressure of 110/70 mmHg in our hospital. Physical examination revealed bilateral enlargement of the thyroid gland that was firm and tender to palpation.

Thyroid function test results in the 12th week of gestation showed the following: serum thyroxine (T4) 122.168 ng/mL (reference range: 50–130 ng/mL); serum triiodothyronine (T3) 1.481 ng/mL (reference range: 0.8–1.9 ng/mL); serum-free thyroxine (FT4) 9.444 pmol/L (reference range: 9.1–24.8 pmol/L); serum-free triiodothyronine (FT3) 4.321 pmol/L (reference range: 3.3–9.15 pmol/L); serum thyroid-stimulating hormone (TSH) 0.149 ulU/mL (reference range: 0.27–4.2 uIU/mL); anti-thyroglobulin antibody < 6% (reference range: < 30); thyroid peroxidase antibody < 5% (reference range: < 34); thyrotropin receptor antibody 4.3 U/L (reference range: < 12); and, ESR 31 mm/h (reference range: 0–20 mm/h) (Table 1, Fig. 1). Thyroid ultrasound showed that the solid area of the left thyroid lobe had low echogenicity, suggesting SAT. Thyroid function test results in the 14th week of gestation were as follows: T4 222.1 ng/mL; T3 3.07 ng/mL; and, TSH 0.058 ulU/mL (Table 1, Fig. 1). Her thyroid function was checked again in the 17th week and the results showed T4 255.4 ng/mL, T3 3.18 ng/mL, and TSH 0.005 ulU/mL( Table 1, Fig. 1).

Table 1 Laboratory data of thyroid function and erythrocyte sedimentation rate
Fig. 1
figure 1

Changes in thyroid function and erythrocyte sedimentation rate. ESR: Erythrocyte sedimentation rate; LT4: Levothyroxine; P: Postpartum; PAT: Prednisone Acetate Tables; TSH: Thyroid-stimulating hormone; TT4: Thyroxine; W: Weeks of gestation

Based on patients symptoms, physical examination and laboratory findings she was diagnosed with SAT. Topical hydrocortisone ointment was given to alleviate the neck pain; however, she developed a fever after 2 days, which peaked at 37.8 ºC, and unbearable neck pain. The pain was so severe that 10 mg per day oral prednisone was administered, which was increased to 15 mg per day 10 days later for unalleviated pain. The patient responded well to the treatment and she was really grateful for her mitigation of her pain. The neck pain disappeared in the 21th week of gestation. The thyroid function test results were as follows: T4 122.63 ng/mL; T3 1.7 ng/mL; and TSH 0.005 ulU/mL (Table 1, Fig. 1). In the 24th week, the results were: T4 110.02 ng/mL; T3 1.81 ng/mL; and TSH 7.18 ulU/mL (Table 1, Fig. 1). Meanwhile, 25 ug levothyroxine was also administered, starting in the 24th week of gestation and was continued throughout the pregnancy. The thyroid function and ESR were normal in the 27th week of gestation (Table 1, Fig. 1) and therefore,prednisone treatment was stopped in the 28th week but levothyroxine was continued. Thyroid function in gestational week 31 showed that TSH level was 3.83 ulU/mL (Table 1, Fig. 1). Therefore, the dose of levothyroxine was increased to 50 ug per day until delivery. Throughout this time the patient’s TSH level was maintained at 2.26–3.01 ulU/mL (Table 1, Fig. 1).

Glucocorticoid levels are high during pregnancy due to an increase in estrogen in the circulation, which promotes the generation of glucocorticoid-binding globulin and increases corticosteroid hormones in the plasma [11]. Importantly, extensive low echogenicity seen on ultrasound is also an essential and sufficient indicator for glucocorticoid use [5]. The patient in this study as well as three reported SAT cases during pregnancy were treated with glucocorticoids, which effectively alleviated the pain of patients [5, 7, 10].

While discontinuing to take her levothyroxine replacement at the 41th week of gestation, the patient gave birth to a healthy baby boy via caesarean section, with a weight of 3600 g and an Apgar score of 9–10. Thyroid function test 2 weeks postpartum were as follows: TSH 2.26 ulU/mL; T4 84.04 ng/mL; and, T3 1.38 ng/mL (Table 1, Fig. 1).

Discussion and conclusion

In general,one or two women suffer from thyrotoxicosis per 1000 pregnancies. Hiraiwa assumed that SAT accounts for 1% of thyrotoxicosis, 10–20 out of one million pregnant women will develop SAT [5]. In this study, we report a case of a pregnant woman with SAT, which is very uncommon,To date, only seven cases have been reported [5,6,7,8,9,10] (Table 2). Therefore, there is a need to carefully manage such cases.

Table 2 Summary and review of case reports in pregnant women with subacute thyroiditis

While the pathogenesis of SAT remains unknown.However, it has been postulated that viral infection leads to the production of an antigen that binds tightly to the human leukocyte antigen-B35 molecule on macrophages, activating cytotoxic T lymphocytes through helper T1 cells (Th1 cells). With the destruction of thyroid follicular cells, thyroid hormone is released into the blood, which results in symptoms of thyrotoxicosis [12]. Further, the hypofunction of iodine upake appears as thyroid follicular cells are destroyed, and the depletion of thyroid hormone is accompanied by hypothyroidism. Most thyroid functions return to normal as patients recover from SAT [9]. During pregnancy, B lymphocytes are inhibited while Th2 cells are activated, which dampen the function of Th1 cells. This may partially explain the low incidence and insignificant clinical symptoms of SAT during pregnancy [13].

SAT diagnosis is based on the patient’s medical history, symptoms, physical and laboratory fingings along with exclusion of other reasons for hyperthyroidism. Our patient presented with SAT symptoms in the 12th week of gestation, in accordance with previously published case reports of SAT during early pregnancy (sixth to 13th week) [5,6,7,8,9,10]. It is important to recognize thyroid dysfunction caused by human chorionic gonadotropin (HCG) in the first trimester. HCG levels increase significantly in early pregnancy and its structure is homologous to TSH, which leads to a transient rise in free thyroxin (FT4) and suppression of TSH; however, there is no neck pain during normal early pregnancy [13].

The physical findings of neck pain favors SAT in the differential diagnosis of SAT from other causes of hyperthyroidism or hypothyroidism during pregnancy. However, in some patients with Hashimoto’s thyroiditis [14], thyroid cancer or primary thyroid lymphoma, or even Graves’ disease may also have neck pain and tenderness of the thyroid gland in some cases. Importantly, all of the previously reported 7 patients with SAT during pregnancy had neck pain. Pain from SAT can be initially confined to or begin from the lateral gland, and then transferred to the contralateral gland [9]. In our case, the patient’s neck pain was found to be transferable and consistent with SAT. Importantly, additional clinical symptoms, such as fever and fatigue, were also observed.

Hyperthyroidism during SAT in pregnant women, manifested as low TSH and increased T3 and T4, needs to be differentiated from Graves’ disease. SAT patients also have a high ESR or CRP but poor radionuclide uptake in thyroid scintigraphy, although fine-needle aspiration biopsy may also be considered as a diagnostic method [13]. Howerver, pregnant women are not recommended to undergo thyroid scintigraphy and fine-needle aspiration biopsy has a higher inherent risk, which may contribute to the challenge of diagnosing pregnancy complicated with SAT..SAT is characterized by a low ratio of TT3 (ng/dL) to TT4 (µg/dL) < 20, FT3 to FT4 < 0.3 [15] and peripheral-blood eosinophil/monocyte (Eo/Mo) ratio < 0.2 [16]. These indicators are valuable for distinguishing SAT from Graves’ disease. In this case, TT3/TT4 = 12.12, FT3/FT4 = 0.46, and Eo/Mo = 0.076, consistent with the literature [15, 16], with the exception of FT3/FT4.

The diagnosis of SAT in pregnancy is based on the patient’s medical history, symptoms, physical and laboratory findings and exclusion of other reasons for thyroid dysfunction. Monitoring of the changes in thyroid hormone may also play an important role in the treatment of SAT.

Availability of data and materials

The datasets analyzed during the current study are not publicly available due to protection of the patient’s privacy but are available from the corresponding author on reasonable request (email: yangying2072@126.com).

Change history

Abbreviations

SAT:

Subacute thyroiditis

ESR:

Erythrocyte sedimentation rate

CRP:

C-reactive protein

T4:

Thyroxine

T3:

Triiodothyronine

FT4:

Serum-free thyroxine

FT3:

Serum-free triiodothyronine

TSH:

Thyroid-stimulating hormone

HCG:

Human chorionic gonadotropin

References

  1. De Groot L, Abalovich M, Alexander EK, Amino N, Barbour L, Cobin RH, et al. Management of thyroid dysfunction during pregnancy and postpartum: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2012;97(8):2543–65. https://0-doi-org.brum.beds.ac.uk/10.1210/jc.2011-2803.

    Article  CAS  PubMed  Google Scholar 

  2. Jin Y, Yang L, Hongjie L, Heming Z, Xiaofeng Li, Lin Z, Zhe W. Associations of maternal iodine status and thyroid function with adverse pregnancy outcomes in Henan Province of China. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 2018;47:104–10. https://0-doi-org.brum.beds.ac.uk/10.1016/j.jtemb.2018.01.013.

  3. Slatosky J, Shipton B, Wahba H. Thyroid: differential diagnosis and management. Am Fam Physician. 2000;61(4):1047–52.

    CAS  PubMed  Google Scholar 

  4. G?rges J, Ulrich J, Keck C, M¨1ller-Wieland D, Diederich S, Janssen OE. Long-term Outcome of Subacute Thyroiditis. Exp Clin Endocrinol Diabetes. 2020;128(11):703–8.DOI:https://0-doi-org.brum.beds.ac.uk/10.1055/a-0998-8035

  5. Hiraiwa T, Kubota S, Imagawa A, Sasaki I, Ito M, Miyauchi A, et al. Two cases of subacute thyroiditis presenting in pregnancy. J Endocrinol Invest. 2006;29(10):924–7. https://0-doi-org.brum.beds.ac.uk/10.1007/BF03349198.

    Article  CAS  PubMed  Google Scholar 

  6. Anastasilakis AD, Karanicola V, Kourtis A, Makras P, Kampas L, Gerou S, et al. A case report of subacute thyroiditis during pregnancy: difficulties in differential diagnosis and changes in cytokine levels. Gynecol Endocrinol. 2011;27(6):384–90. https://0-doi-org.brum.beds.ac.uk/10.3109/09513590.2010.493963.

    Article  CAS  PubMed  Google Scholar 

  7. Singh I, El-Maouche D, et al. Subacute Thyroiditis Masquerading as Hyperemesis Gravidarum in Early Pregnancy. Clin Thyroidol. 2015;27:346–50. https://0-doi-org.brum.beds.ac.uk/10.1089/ct.2015;27.346-350.

    Article  Google Scholar 

  8. Yildiz C, Altay M, Pregnancy STD. J Contemp Med. 2017. https://0-doi-org.brum.beds.ac.uk/10.16899/gopctd.302434.

  9. Li Y, Honghua Wu, Gao Y, Guo X. Clinical treatment of pregnancy complicated with subacute thyroiditis. Chinese Journal of Endocrinology and Metabolism. 2012;28(8):673–5. https://0-doi-org.brum.beds.ac.uk/10.3760/cma.j.issn.1000-6699.2012.08.017.

    Article  Google Scholar 

  10. M. A. Kaykhaei,T. Mohammadi Fatideh,M. Sooghi.A case of subacute Thyroiditis in the first trimester of pregnancy[J].Acta endocrinologica: the international journal of the Romanian Society of Endocrinology,2012;8(1):125–130.DOI:https://0-doi-org.brum.beds.ac.uk/10.4183/aeb.2012.125

  11. Chi CC, Kirtschig G, Aberer W, Gabbud JP, et al. Evidence-based (S3) guideline on topical corticosteroids in pregnancy. Br J Dermatol. 2011;165(5):943–52. https://0-doi-org.brum.beds.ac.uk/10.1111/j.1365-2133.2011.10513.x.

    Article  CAS  PubMed  Google Scholar 

  12. Weetman AP, Smallridge RC, Nutman TB, Burman KD. Persistent thyroid autoimmunity after subacute thyroiditis. J Clin Lab Immunol. 1987;23:1–6.

    CAS  PubMed  Google Scholar 

  13. Lazarus JH. Thyroid disorders associated with pregnancy: etiology, diagnosis, and management. Treat Endocrinol. 2005;4:31–41. https://0-doi-org.brum.beds.ac.uk/10.2165/00024677-200504010-00004.

    Article  PubMed  Google Scholar 

  14. Kon YC, DeGroot LJ. Painful Hashimoto’s thyroiditis as an indication for thyroidectomy: clinical characteristics and outcome in seven patients. J Clin Endocrinol Metab. 2003;88(6):2667–72. https://0-doi-org.brum.beds.ac.uk/10.1210/jc.2002-021498.

  15. Amino N, Yabu Y, Miki T, Morimoto S, Kumahara Y, Mori H, et al. Serum ratio of triiodothyronine to thyroxine, and thyroxine-binding globulin and calcitonin concentra tions in Graves’ disease and destruction-induced thyrotoxicosis. J Clin Endocrinol Metab. 1981;53(1):113–6. https://0-doi-org.brum.beds.ac.uk/10.1210/jcem-53-1-113.

  16. Izumi Y, Hidaka Y, Tada H, Takano T, Kashiwai T, Tatsumi KI, et al. Simple and practical parameters for differentiation between destruction-induced thyrotoxicosis and Graves' thyrotoxicosis. Clin Endocrinol(Oxf).2002;57(1):51–8.DOI:https://0-doi-org.brum.beds.ac.uk/10.1046/j.1365-2265.2002.01558.x

  17. Gagnier JJ, Kienle G, Altman DG, Moher D, Sox H, Riley D, et al. The CARE guidelines: consensus-based clinical case reporting guideline development. Glob Adv Health Med. 2013;2:38–43. https://0-doi-org.brum.beds.ac.uk/10.7453/gahmj.2013.008.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We would like to thank the patient and her family for consenting to publish this case report.

Funding

This work was supported by grants from the Natural Science Foundation of China (No. 81760734, No. 81770384 and No. 31660313), Natural Science Foundation of Yunnan Province (No.2017FA048), Fund of Diabetic Innovation Team (No. 2019HC002), Endocrine Clinical Medical Center of Yunnan Province (No. ZX2019-02–02), Fund of Medical Leader in Yunnan Province (No. L-201609), Association Foundation Program of Yunnan Provincial Science and Technology Department and Kunming Medicine University (No. 202101AY070001-199). With the support of these funds, we were able to design the study and complete the data collection and analysis.

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Authors

Contributions

CFB, GHS, YY, and KY contributed to the conception of the study; CFB and GHS contributed to drafting of the manuscript; YYZ, XQG helped conduct the analyses and provided constructive discussion; KY and YY were involved in designing the study, revising the manuscript, and supervising the work;MRH provided language revision and overall revision the manuscript; All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ying Yang.

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Written consent was obtained from the patient to participate. According with The CARE Guidelines, case reports do not need ethics committee approval [17].

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Written informed consent for publication was obtained from the patient.

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The authors declare that they have no competing interests.

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Bai, CF., Shen, GH., Yang, Y. et al. Subacute thyroiditis during early pregnancy: a case report and literature review. BMC Pregnancy Childbirth 22, 19 (2022). https://0-doi-org.brum.beds.ac.uk/10.1186/s12884-021-04368-2

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