Since 1942, therapy with radioiodine ((NaI)-I-131) has gained a major role
in the treatment of benign thyroid disorders, notably hyperthyroidism cause
d by Graves' disease or toxic multinodular goiter. The very large series of
patients treated so far offer the opportunity for an assessment of both be
nign and malignant side effects. Hyperthyroidism is sometimes observed afte
r radioiodine therapy due to radiation induced thyroid hormone or by an imm
unological mechanism. Despite the numerous attempts to design dosage schedu
les aiming at euthyroidism, hypothyroidism occurs in the majority of patien
ts throughout life. Transient hypothyroidism may be observed within the fir
st year after therapy and is caused by an immunological mechanism. Radioiod
ine therapy in Graves' disease may induce or worsen ophthalmopathy, which c
an be prevented by steroids effectively. Hypoparathyroidism and hyperparath
yroidism have been reported after radioiodine therapy but probably do not e
xceed the normal incidence. Sialitis is commonly observed but mostly in pat
ients treated with radioiodine for thyroid cancer. There are no indications
for induction of genetic abnormalities after radioiodine therapy although
no definite conclusion can be reached. Much attention has been paid to mali
gnant disease. In very large series, no effects of radioiodine therapy on s
urvival have been observed. Some studies report an increased relative risk
for certain types of cancer (notably thyroid cancer, stomach cancer, bladde
r and kidney cancer or hematological malignancies). However, these observat
ions were not confirmed by other large studies, so that no definite conclus
ion with respect to risk for certain types of malignant disease can be draw
n. However, radioiodine therapy for benign thyroid disorders has generally
been considered safe and without major side effects, hypothyroidism being t
he most frequent one.