Summary
OBJECTIVE Although non‐toxic diffuse goitre is a common disorder, little is known of the clinical course of patients. We therefore decided to investigate the long‐term clinical outcome of patients with non‐toxic diffuse goitre.
DESIGN A retrospective study.
PATIENTS Of 850 patients with non‐toxic diffuse goitre who met our criteria and were seen in our thyroid clinic between 1977 and 1985, 108 who had been followed for from 5 to 14 years (mean 8 years) were entered in this study. All patients fulfilled our criteria having soft diffuse goitres, normal serum TSH and T4 concentrations, and undetectable antithyroglobulin and antithyroid microsomal antibodies.
MEASUREMENTS A family history of thyroid disease was obtained and the occurrence of Graves' ophthalmopathy was noted. Serum TSH and T4 concentrations, and antithyroglobulin and antithyroid microsomal antibodies were measured during the follow‐up period. Thyroidal radioactive iodine uptake (RAIU), serum free T4 and free T3 concentrations, and TSH binding inhibitory immunoglobulin (TBII) activities were determined in all patients who were subsequently found to have abnormal serum TSH or T4 concentrations or signs of Graves' ophthalmopathy.
RESULTS Thirty‐six of the 108 patients (33%) had a family history of autoimmune thyroid disease. Elevated serum T4 or free T4 concentrations and depressed serum TSH concentrations were found in six patients during the follow‐up period. Hyperthyroid Graves' disease was diagnosed in four of the six patients, subacute thyroiditis in one, and transient post‐partum thyrotoxicosis in one. Hypothyroidism was found in one patient who was diagnosed as having transient post‐partum hypothyroidism. Euthyroid Graves' disease was diagnosed in one patient. Furthermore, six of these eight patients had a family history of autoimmune thyroid disease in first‐degree relatives.
CONCLUSION During a prolonged follow‐up period of patients with non‐toxic diffuse goitre, Graves' disease was found in five of 108 patients (four hyperthyroid Graves' and one euthyroid Graves'), post‐partum thyroid dysfunction in two, and subacute thyroiditis in one. Six of these eight patients had a family history of autoimmune thyroid disease in first‐degree relatives. Long‐term follow‐up is necessary for patients with non‐toxic diffuse goitre, especially those who have a family history of autoimmune thyroid disease.