Hb. Burch et al., DIAGNOSIS AND MANAGEMENT OF THE AUTONOMOUSLY FUNCTIONING THYROID-NODULE - THE WALTER-REED-ARMY-MEDICAL-CENTER EXPERIENCE, 1975-1994, Thyroid, 8(10), 1998, pp. 871-880
In order to characterize the clinical and laboratory features of auton
omously functioning thyroid nodules (AFTNs), and to assess optimal dia
gnosis and management of patients with this disorder, we performed a r
etrospective analysis of 49 such patients over a 22-year period encomp
assing January 1975 to November 1996. The following data were analyzed
: thyroid hormone levels, thyroid scintiscan, radioiodine uptake, fine
-needle aspiration biopsy, triiodothyronine (T-3) suppression testing,
thyrotropin-releasing hormone (TRH) stimulation test, and thyroid ult
rasound. Clinical outcomes assessed included persistent hyperthyroidis
m, hypothyroidism, and nodule shrinkage after treatment, or in patient
s followed without definitive therapy, nodule growth, spontaneous dege
neration, and progression to hyperthyroidism. Biochemical hyperthyroid
ism, often subclinical, was found in 73.5% of patients at presentation
and in an additional 24.4% of patients during subsequent follow-up. T
he introduction of sensitive thyrotropin (TSH) testing during the peri
od of study resulted in a decrease in the use of the T-3-suppression t
est and TRH stimulation test from 100% and 20%, respectively, in the p
eriod from 1976-1980, to 4% each in the period from 1991-1996. T-3-thy
rotoxicosis occurred in 12.2% of patients. Thyrotoxicosis at any time
during the course of follow-up was positively correlated with nodule s
ize at diagnosis. Definitive therapy, used in 42.8% of patients, consi
sted of radioiodine ablation (38.1%) or thyroidectomy (61.9%). No pati
ent had recurrence of thyrotoxicosis after definitive therapy, but 25%
became hypothyroid. During follow-up for a mean of 30.9 months, nodul
es enlarged in 25% of patients overall, or 33% of patients not receivi
ng definitive therapy. Cystic degeneration was documented in 26.5% of
patients, although this change rarely reversed subclinical hyperthyroi
dism. The diagnosis of an AFTN requires a demonstration of TSH-indepen
dent nodular hyperfunction. The introduction of sensitive TSH assays h
as simplified the evaluation of AFTN patients and revealed a high prev
alence of subclinical thyroid hyperfunction in this disorder. In view
of current increased awareness of adverse consequences associated with
subclinical hyperthyroidism and the rarity of spontaneous resolution
of hyperthyroidism in AFTN patients (despite a propensity for spontane
ous hemorrhage), definitive therapy is recommended. Both radioiodine a
nd hemithyroidectomy have high cure rates and a low posttreatment inci
dence of hypothyroidism.