Journal List > J Korean Soc Endocrinol > v.20(3) > 1063787

Kong, Joo, Shin, Na, An, Kang, Park, Son, Kim, and Kim: A Case of Thyroid MALT Lymphoma without Autoimmune Thyroiditis

Abstract

A primary thyroid lymphoma is rare among all types of thyroid malignancy. Usually, a thyroid lymphoma is associated with underlying chronic autoimmune thyroiditis. Recently, we experienced a primary thyroid mucosa-associated lymphoid tissue (MALT) lymphoma, with an incidental micropapillary thyroid carcinoma, but lacking evidence of autoimmune thyroiditis. A female patient visited our hospital for further evaluation of a rapidly enlarging, painless thyroid mass which had been stable for 8 years. Lymphocytic thyroiditis or a lymphoma was suspected from fine needle aspiration performed at another hospital. The thyroid function test and other routine laboratory tests were normal. The histopathological findings after a total thyroidectomy revealed a MALT lymphoma with a micropapillary thyroid carcinoma. There was no evidence of chronic autoimmune thyroiditis. This is, to the best of our knowledge, the first case report of a MALT lymphoma arising from the thyroid gland without evidence of chronic autoimmune thyroiditis in Korea

Figures and Tables

Fig. 1
Computed tomography of the neck shows soft tissue mass in isthmus of thyroid gland (arrow)
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Fig. 2
Sections from thyroid gland showing proliferation of multiple lymphoid follicles with intervening thyroid follicular epithelial cells (H-E, ×40)
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Fig. 3
Atypical lymphoid cells infiltrating thyroid follicular cells, so-called lymphoepithelial lesions are seen (H-E, ×200)
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Fig. 4
Atypical lymphoid cells are positive for CD20 (IHC, ×200)
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Fig. 5
Sections from thyroid gland showing typical histologic features of papillary carcinoma (H-E, ×100)
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