ESPE2016 Poster Presentations Thyroid P2 (49 abstracts)
aRoyal Childrens Hospital, Melbourne, Victoria, Australia; bMurdoch Childrens Research Institute, Melbourne, Victoria, Australia
Background: Neonatal hyperthyroidism is a rare condition seen in infants born to mothers with Graves disease, with transplacental transfer of TSH receptor antibodies (TRAb) to the baby. Some patients have been shown to swing from hypothyroidism to hyperthyroidism as TSH receptor blocking and stimulating antibodies may coexist.
Objective and hypotheses: To describe a rare clinical event of a neonate with severe Graves hyperthyroidism, born to a mother with autoimmune hypothyroidism
Method: A baby boy born preterm at 35 weeks gestation had significant irritability, tachycardia and a suspicion of proptosis 36 hours after birth. The mother was known to have autoimmune hypothyroidism, diagnosed at age ten and was taking levo-thyroxine replacement with normal thyroid function throughout this pregnancy. She had never been thyrotoxic. She also had pernicious anaemia and extensive vitiligo. Her sister and grandmother have Hashimotos thyroiditis. Her mother has Graves disease. The mother therefore was tested for TRab.
Results: The babys thyroid function on day 3 demonstrated gross thyrotoxicosis, TSH<0.01 mU/l (NR day 3 <10 mU/l), FT4 >77 pmol/l (2035) and FT3 15.4 pmol/l. TRab was elevated at 18.4 IU/l (<1.8). The mothers TRab was high at 24.7 IU/l. The baby was commenced on propranolol on day 7, with some symptomatic improvement, however thyroid hormones continued to rise. After endocrine consultation, on day 17 carbimazole (CBZ) was commenced, at 0.3 mg/kg per day. Thyroid function normalized within 10 days, CBZ was gradually tapered and medication was weaned by 7 weeks. He has remained euthyroid. His mother continues to require replacement thyroxine.
Conclusion: Rare cases of de novo development of TSH stimulating antibodies are described in patients on levothyroxine and might provide an explanation for our case. However, almost all infants reported with neonatal thyrotoxicosis were either de novo or associated with maternal history of active or treated Graves disease.1 Our findings have important implications for future follow up of this family and for management of future pregnancies.