A 3-year-old girl with Graves' disease with literature review

Yo Han Ho1, Eun Cho Chung1, Sin-Ae Park1

  • 1Department of Pediatrics, Presbyterian Medical Center, Jeonju, Korea.

Insights

This case report details Graves' disease in a 3-year-old, highlighting its rarity in young children. Early diagnosis and treatment are crucial for managing pediatric hyperthyroidism and preventing developmental issues.

Area of Science:

  • Pediatric Endocrinology
  • Autoimmune Diseases

Background:

  • Graves' disease is the primary cause of hyperthyroidism in children.
  • It is exceptionally rare in children under 4 years old.
  • Untreated hyperthyroidism can impede growth and development.

Purpose of the Study:

  • To report the first case of Graves' disease in a child under 4 years old in Korea.
  • To emphasize the importance of recognizing and treating this condition in very young children.

Main Methods:

  • Case presentation of a 3-year-old girl with symptoms of hyperthyroidism.
  • Laboratory tests including thyroid hormones (T3, free T4, TSH), antimicrosomal antibody, and TSH-binding inhibitory immunoglobulin.
  • Thyroid scan to assess gland size and function.

Main Results:

  • The patient presented with goiter, exophthalmos, heat intolerance, and hyperactivity.
  • Initial thyroid hormone levels were normal, but TSH was decreased.
  • Elevated antimicrosomal antibody and TSH-binding inhibitory immunoglobulin levels were detected.
  • Thyroid scan revealed diffuse enlargement and increased uptake.
  • Hyperthyroidism developed 3 months after initial presentation.
  • The patient was diagnosed with Graves' disease and treated with methimazole.

Conclusions:

  • Graves' disease can occur in children younger than 4 years old.
  • This case represents the first documented instance in Korea.
  • Prompt diagnosis and management are essential for affected children.

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