@Article{Chemperek2006,
journal="Reumatologia/Rheumatology",
issn="0034-6233",
volume="44",
number="6",
year="2006",
title="Case reportAmyloid goiter as the evidence in secondary amyloidosis in a patient with rheumatoid arthritis",
abstract="Amyloidosis represents not a single disease but a group of diverse pathological processes which can affect any organ or tissue in the body. AA amyloidosis occurs secondary to chronic infections or as a complication from tissue injury, recurrent long-standing inflammatory and autoimmune diseases, most frequently rheumatoid arthritis. Amyloid goiter is an extremely rare condition associated with a clinically apparent enlargement of the thyroid due to massive amyloid infiltration. Amyloid deposition in secondary amyloidosis frequently involves the thyroid gland, but rarely results in a clinically palpable goiter. Expanding mass can cause dyspnoea, dysphagia and hoarseness. We present a 57-year-old woman with amyloid goiter due to rheumatoid arthritis, who developed thyrotoxicosis resembling Hashimoto\&#8217;s thyroiditis. She noticed neck swelling with severe neck tenderness, palpitations, hyperhydrosis and weight loss. Her serum free T4 and T3 were high, TSH was suppressed to subnormal, anti-thyroid autoantibodies were positive. Surgical therapy is aimed at avoidance of the existing and threatening consequences of expanding mass. The diagnosis of amyloid goiter should be suspected in patients with a diffusely enlarging thyroid gland and an appropriate clinical history.",
author="Chemperek, Ewa
and Majdan, Maria
and Kurowska, Maria
and Piotrowski, Mariusz",
pages="374--377",
url="https://www.termedia.pl/Case-report-Amyloid-goiter-as-the-evidence-in-secondary-amyloidosis-in-a-patient-with-rheumatoid-arthritis,18,7274,1,1.html"
}