Nodular pretibial myxoedema after treatment of Graves disease with radioactive iodine ablation therapy.
نویسندگان
چکیده
To cite: Ponnusamy D, Ramachandra Pai RP. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013202530 DESCRIPTION A 45-year-old African-American woman presented with a 2-month history of bulging eyes, neck swelling, increased appetite and oligomenorrhea. On examination, she had fine hand tremors and bilateral proptosis with lid lag. The thyroid gland was diffusely enlarged. Laboratory test revealed suppressed thyrotropin-stimulating hormone and elevated free thyroxine levels at 7.4 ng/dL (normal 0.76–1.46 ng/dL). She was diagnosed with Graves disease and treated with 15.3 mCi of radioactive iodine therapy. She had normalisation of thyroid function tests after the treatment. Eight months later, she noted multiple, nontender, raised nodular lesions in her shins bilaterally (figure 1A). Differential diagnosis included chronic erythema nodosum and nodular form of pretibial myxoedema. Biopsy was performed and cytopathology revealed marked dermal mucin, consistent with pretibial myxoedema (figure 1B). She was prescribed clobetasol ointment for her lesions. Dermopathy occurs in less than 5% of patients with Graves disease. Typical lesion is diffuse, non-pitting oedema with ‘orange-skin’ appearance involving the shins. Nodular lesions are rare, in less than 10% of patients with pretibial myxoedema. This case emphasises the atypical signs of Graves disease and changes that can occur in the skin even after Graves disease has been successfully treated. Physicians following patients with Graves disease after definitive management of the same should be aware of this rare form of thyroid dermopathy.
منابع مشابه
Iatrogenic myxoedema madness following radioactive iodine ablation for Graves' disease, with a concurrent diagnosis of primary hyperaldosteronism
UNLABELLED Myxoedema madness was first described as a consequence of severe hypothyroidism in 1949. Most cases were secondary to long-standing untreated primary hypothyroidism. We present the first reported case of iatrogenic myxoedema madness following radioactive iodine ablation for Graves' disease, with a second concurrent diagnosis of primary hyperaldosteronism. A 29-year-old woman presente...
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ورودعنوان ژورنال:
- BMJ case reports
دوره 2014 شماره
صفحات -
تاریخ انتشار 2014