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Endocrine Abstracts (2025) 110 EP1619 | DOI: 10.1530/endoabs.110.EP1619

1Faculty of Medecine of Sousse, University of Sousse, Sousse, Tunisia


JOINT3619

Introduction: Subacute thyroiditis of Quervain is an acute inflammatory condition of the thyroid, most likely triggered by a viral infection. Its prevalence is estimated to be around 0.1% to 0.5% of the general population, making it relatively rare compared to other types of thyroiditis.

Case report: A 55-year-old female patient with no significant medical history who presented with a cervical swelling. Ultrasound examination revealed a thyroid nodule classified as EUTIRADS 4, with a Bethesda II on fine-needle aspiration cytology. In June 2024, the patient developed flu-like symptoms followed by the onset of a painful, vascular goiter in the context of a febrile illness. Laboratory investigations showed an inflammatory syndrome with a CRP of 179, and hyperthyroidism (TSH 0.02 mIU/l, FT4 36 pmol/l). The patient was treated with anti-inflammatory drugs for one month, resulting in significant improvement of the pain. Subsequent tests two months after the first episode revealed a hypothyroidism with a TSH of 87 mIU/l and FT4 of 3.6 pmol/l. Ultrasound imaging confirmed the presence of a goiter with features suggestive of acute thyroiditis. Levothyroxine therapy was initiated. Six months after this episode, the patient re-presented with the same plaints: bilateral neck pain and odynophagia. Examination revealed a tender goiter, with a CRP of 92 and an elevated erythrocyte sedimentation rate (ESR) of 91 mm/h and a TSH level at 13 mUI/l, confirming the recurrence of the Subacute thyroiditis.

Conclusion: The Quervain’s thyroiditis typically follows a course of three phases: an initial hyperthyroid phase, followed by a hypothyroid phase, and eventual spontaneous recovery within two to three months, with recurrence being rare, occurring in only 1.4% to 10% of cases. These recurrences are mainly due to the inflammatory origin of this pathology, the underlying inflammation may persist or reactivate, potentially causing a recurrence of the disease. Additionally, factors such as genetics, the immune system, and recurrent viral infections could contribute to this reactivation.

Volume 110

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

European Society of Endocrinology 
European Society for Paediatric Endocrinology 

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