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Endocrine Abstracts (2025) 110 P1180 | DOI: 10.1530/endoabs.110.P1180

ECEESPE2025 Poster Presentations Thyroid (141 abstracts)

The coexistence of graves’ disease and thymic hyperplasia: a case report

Megi Lekbello 1 , Marjeta Kermaj 1 & Dorina Ylli 2


1University Hospital "Mother Tereza", Endocrinology, Tirana, Albania; 2University of Medicine, Tirana, Albania


JOINT2886

Introduction: Thymic hyperplasia is frequently observed in patients with Graves’ disease. The association between Graves’ disease and thymic hyperplasia was first described in 1912, and up to 38% of patients with Graves’ disease exhibit histological thymic abnormalities. However, the exact mechanism underlying the development of thymic hyperplasia in these patients remains unclear.

Case Report: We present a case report of a 23-year-old female medical student who presented to the outpatient clinic with complaints of palpitations, tachycardia, tremors, anxiety, and a weight loss of 5 kg over three months. She had no eye symptoms. On physical examination, her vital signs were as follows: blood pressure of 110/70 mmHg, heart rate of 130 beats per minute, respiratory rate of 18 breaths per minute, weight of 49 kg, and height of 160 cm (body mass index of 19.14 kg/m2). Laboratory tests revealed a suppressed TSH level of <0.005 μIU/mL (reference range: 0.27–4.2 μIU/mL), elevated free T4 of 4.47 ng/dl (reference range: 0.93–1.7 ng/dl), thyroperoxidase antibody of 397 IU/mL (reference range: 0–34 IU/mL), and thyrotropin-binding inhibitory immunoglobulins of 37 IU/l (reference range: 0–115 IU/l). The anti-TSH receptor antibody was also elevated at 20.5 IU/l (reference range: <1.22 IU/l). A thyroid ultrasound showed a heterogeneous and hypoechoic thyroid gland with increased vascularization. Additionally, a heterogeneous structure was observed below the left thyroid lobe. A CT scan of the neck and chest confirmed the presence of a hyperplastic thymus measuring 27 mm, located below the thyroid gland. Following a neurological evaluation, electromyography (EMG) was performed, and myasthenia gravis was ruled out. The patient was started on Methimazole 5 mg twice daily (2-0-2). After six weeks, she returned for follow-up with no symptoms of hyperthyroidism and a weight gain of 1.5 kg. Laboratory results showed TSH at 0.45 μIU/mL and free T4 at 1.1 ng/dl. A follow-up neck CT scan was scheduled for three months later.

Conclusion: Thymic hyperplasia is a common finding in patients with Graves’ disease. It is important to consider this diagnosis in patients with thyrotoxicosis and a mediastinal mass to prevent unnecessary interventions that could lead to harm. The prognosis is excellent, and treatment with methimazole has been reported to contribute to thymic mass reduction.

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 
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