A fetal goiter is an enlargement of the thyroid gland in utero. It can occur with either hyper- or hypothyroidism (and in isolated cases of euthyroidism 8).
On this page:
Pathology
The mechanism depends on whether the underlying cause is hyper- or hypothyroidism.
Associations
maternal Graves disease with propylthiouracil (PTU) treatment 1
polyhydramnios: from impaired swallowing 2
Radiographic features
Ultrasound
While antenatal detection is rare, once detected, it is important to evaluate fetal thyroid function in order for early treatment to be initiated if necessary.
A fetal goiter may be seen as a relatively homogeneous anterior fetal neck mass. There is also evidence of polyhydramnios. If the goiter is very large the neck may appear hyperextended.
Some investigators have attempted to assess the hyper- or hypothyroid status relying on sonographic features 7:
-
hypothyroid goiters
more likely to have a peripheral vascular pattern on color Doppler
may have evidence of delayed bone maturation
may be accompanied by increased fetal movement
-
hyperthyroid goiters
more likely to have central vascularization
may have evidence of a fetal tachycardia
may have evidence of advanced bone maturity
Treatment and prognosis
Treatment will, again, depend on whether the fetus is hyper- or hypothyroid.
Complications
hydrops fetalis: from increased vascular shunting within the goiter
development of a fetal tachycardia
cervical dystocia: from the extended position of the fetal head in labor