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Endocrine Abstracts (2024) 99 EP602 | DOI: 10.1530/endoabs.99.EP602

1University Hospital Taher Sfar, Endocrinology and Internal medicine Department, Mahdia, Tunisia


Background: Marine-Lenhart syndrome (MLS) is defined by the coexistence of Graves’ disease and a hyperactive nodule or multinodular goiter. Although rare, its diagnosis by functional imaging coupled with ultrasound is necessary in order to propose a radical treatment. We report the case of a patient followed for hyperthyroidism related to a SML.

Case presentation: A 52-year-old patient consulted for a picture of thyrotoxicosis associating tremor, weight loss, polyphagia, irritability and thermophobia. Physical examination revealed a small goiter with a right lobar nodule and bilateral exophtalmia. Hormonal assessment showed a TSH at 0.002 mIU/l and FT4 at 47.1 pmol/l confirming peripheral hyperthyroidism. Anti-TSH receptor antibodies were positive at 40. The Graves’ disease was diagnosed confronted to the proptosis and the positivity of the antibodies. Neck ultrasound showed a hypervascularized goiter and two right lobar nodules classified EU-TIRADS III measuring 7.1 mm and 2.3 mm respectively. Scintigraphy showed an increased diffuse iodine uptake of the thyroid gland along with a partially extinctive thyroid nodule. The patient was put on 20 mg/d of thiamazol in preparation for a radical treatment by total thyroidectomy

Conclusions: The diagnosis of MLS is present in 2-4% of patients with MB; hence the inecessity of a neck ultrasound even in the presence of clinically or biologically obvious Graves’ disease, especially in the presence of a thyroid nodule. Scintigraphy is also required to characterize the nodule. The treatment of MLS is surgical, since resistance to synthetic antithyroid drugs is noted in these cases.

Volume 99

26th European Congress of Endocrinology

Stockholm, Sweden
11 May 2024 - 14 May 2024

European Society of Endocrinology 

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