A case of a girl with Arnold-Chiari type 1 malformation with precocious puberty

  • Min Sun Kim
  • , Pyoung Han Hwang
  • , Dae Yeol Lee*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

A small percentage of individuals have the neurological anomaly of central precocious puberty (CPP). Common neurologic causes of CPP include a tumor or congenital lesions. Although Arnold-Chiari malformation can be caused by congenital or acquired causes, it is unusual in patients with CPP. We present the case of a girl aged 4.5 years who complained of breast budding. Her neurological examination and growth pattern were normal. She had no endocrinological abnormality, except for true precocious puberty. We performed brain magnetic resonance imaging, which showed an Arnold-Chiari type 1 malformation. Currently, this case represents the youngest girl who exhibited both Arnold-Chiari type 1 malformation and precocious puberty. Furthermore, it is likely that there is a meaningful association between the brain lesion and precocious puberty in this case.

Original languageEnglish
Pages (from-to)54-56
Number of pages3
JournalKorean Journal of Family Medicine
Volume39
Issue number1
DOIs
StatePublished - 2018.01.1

Keywords

  • Arnold-Chiari malformation
  • Child
  • Precocious puberty

Quacquarelli Symonds(QS) Subject Topics

  • Medicine

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