Van Wyk–Grumbach Syndrome: A Rare Manifestation of Juvenile Hypothyroidism
Background Van Wyk–Grumbach (VWG) syndrome is a rare complication of juvenile hypothyroidism characterized by precocious puberty, delayed bone age, and ovarian cysts. Case presentation We report the case of an 8-year-old girl who presented with intermittent vaginal bleeding and abdominal pain. Imaging revealed bilateral multiseptate ovarian cystic lesions. She had been advised to undergo surgical management at a community health center and was subsequently referred to our institution. Following comprehensive clinical, radiological, and biochemical evaluation, a diagnosis of VWG syndrome was established. Conclusion VWG syndrome should be considered in pediatric females with bilateral ovarian enlargement and precocious puberty, particularly in the context of delayed bone age and hypothyroidism. Prompt thyroid hormone replacement can prevent unnecessary surgical procedures.
Authors
- Madhuri Pundlikrao Udgire
- Varun Vasant Nimje
Institutions
- Government of Maharashtra (IN)
- Government Medical College (IN)
- Government Medical College (IN)
Publication Details
- Journal
- Indian journal of clinical medicine
- Published
- 2026-03-11
- DOI
- https://doi.org/10.1177/26339447261428785
- Primary Topic
- Genetic Syndromes and Imprinting
- Type
- article
- Field-Weighted Citation Impact
- 0.00