Spontaneous Regression of Severe Acquired Infantile Hypothyroidism Associated With Multiple Liver Hemangiomas

Author:

Konrad Daniel1,Ellis Graham2,Perlman Kusiel1

Affiliation:

1. Division of Endocrinology

2. Department of Biochemistry, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

Abstract

A 9-week-old infant presented with severe postnatal hypothyroidism. His hypothyroidism corrected only after his l-thyroxine dose was progressively increased to 28 μg/kg/d. At 6 months of age, multiple clinically asymptomatic hepatic hemangiomas were detected and support a diagnosis of consumptive hypothyroidism as a result of increased type 3 iodothyronine deiodinase activity in the hemangiomas. Coincident with the involution of the hemangiomas, the child’s hypothyroidism improved and l-thyroxin replacement could be stopped at the age of 3 years. Despite some degree of hypothyroidism for several weeks during infancy, his growth and development have been normal.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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1. Multifocal infantile hemangiomas in a 4-month-old female infant;Journal of Skin and Sexually Transmitted Diseases;2024-01-18

2. Consumptive Hypothyroidism due to Hepatic Hemangiomas: A Case Series and Review of the Literature;JPGN Reports;2022-11

3. New approaches for solving the old problem;Pediatric Hematology/Oncology and Immunopathology;2022-03-29

4. Vascular Disorders of the Liver;Textbook of Pediatric Gastroenterology, Hepatology and Nutrition;2021-11-25

5. Infantile hemangioma explained in simple terms;Pediatric Hematology/Oncology and Immunopathology;2021-04-21

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