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Multiple infantile hepatic hemangiomas leading to consumptive hypothyroidism successfully treated with propranolol: A
Anjali Verma1, Rashika Jain1, Neha Babbar1
1Departmentof Pediatrics, PGIMS, Rohtak, Haryana, India.
Insights
Infants with unexplained hypothyroidism may have hepatic hemangiomas that increase deiodinase activity. Treating these liver hemangiomas with propranolol can restore normal thyroid levels.
Area of Science:
- Pediatric Endocrinology
- Vascular Biology
- Hepatology
Background:
- Hepatic hemangiomas are common benign liver tumors in infants.
- Acquired hypothyroidism is a rare complication of hepatic hemangiomas.
- Infant hypothyroidism can lead to developmental issues if untreated.
Observation:
- A 4-month-old infant with multiple hepatic hemangiomas developed acquired hypothyroidism resistant to treatment.
- The infant was born to a diabetic mother.
- Hepatic hemangiomas were suspected to increase type 3 deiodinase activity, converting thyroid hormones T4 to rT3 and T3 to T2.
Findings:
- Treatment of hepatic hemangiomas with propranolol led to tumor regression.
- The infant achieved euthyroidism after hemangioma treatment.
- This suggests a direct link between hepatic hemangiomas and acquired hypothyroidism via deiodinase activity.
Implications:
- Screening for hepatic hemangiomas is recommended for infants with congenital hypothyroidism unresponsive to thyroxine therapy.
- Early propranolol treatment for hepatic hemangiomas may prevent growth retardation and intellectual deficits.
- This case highlights the importance of considering rare causes of endocrine dysfunction in infants.
Abstract:
Hepatic hemangioma is a commonly encountered benign vascular tumour of liver during infancy. Acquired hypothyroidism is one of the rare manifestation of this entity. We report a 4-month-old infant born to a diabetic mother who developed acquired hypothyroidism not responding to treatment due to multiple hepatic hemangiomas. The mechanism behind is increased type 3 deiodinase activity due to hemangiomas of liver, which catalyses conversion of T4 to rT3 and T3 to T2. Hemangiomas were successfully treated with propranolol which lead to its regression and ultimately resulted in euthyroidism. Hence, screening for hepatic hemangioma should be done in all cases of congenital hypothyroidism not responding to thyroxine treatment. We also propose early initiation of treatment of hemangiomas with propranolol as the first line therapy to prevent growth retardation and intellectual loss.
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