Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2010) 24 P48

BSPED2010 Poster Presentations (1) (59 abstracts)

A rare complication of Hashimoto’s thyroiditis

K Kiriella & J Raine


Whittington Hospital, London, UK.


Primary thyroid gland lymphomas account for less than 5% of all thyroid malignancies. They mainly occur in the setting of lymphocytic thyroiditis or Hashimoto’s disease. The majority are mucosa-associated lymphoid tissue lymphomas and diffuse large B-cell lymphomas. There have not been any cases of thyroid lymphoma reported in children in the last 20 years.

Our patient is a 9-year-old boy who was noted to have a lump on the right side of his neck in November 2009. He was initially treated with oral antibiotics for a coexisting upper respiratory tract infection. As there was no improvement, he had thyroid function tests performed. TSH was 55.17 mIU/l and FT4 was 10.1 pmol/l. Thyroid Peroxidase antibodies were 74 IU/ml. He was commenced on Thyroxine. An USS showed an irregular and inhomogeneous mass in the right lobe of the thyroid gland measuring 4 cm×4 cm. Fine needle aspiration showed a thyroid lymphoma arising on a background of chronic lymphocytic thyroiditis.

As the mass rapidly increased in size, he was commenced on Prednisolone, which led to a reduction in the size of the mass. Bilateral bone marrow aspirates, trephine and CSF were negative. He had a CT scan of the neck and chest and a further biopsy which confirmed a B cell lymphoma showing a high proliferation index. He underwent hemithyroidectomy in April 2010. Histopathology revealed a residual necrotic nodule and Hashimoto’s thyroiditis. He has since completed treatment on the B-Non Hodgkin’s lymphoma protocol. In June 2010, he developed type 1 diabetes mellitus. He was positive for Islet cell antibodies but had normal GAD antibodies. He is currently on a basal bolus regimen.

We present a case of a thyroid lymphoma in a patient with Hashimoto’s thyroiditis. It is important to be aware of this rare complication and its association with other autoimmune disorders.

Volume 24

38th Meeting of the British Society for Paediatric Endocrinology and Diabetes

British Society for Paediatric Endocrinology and Diabetes 

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