Kim Min Sun, Hwang Pyoung Han, Lee Dae-Yeol
Department of Pediatrics, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk National University-Biomedical Institute of Chonbuk National University Hospital, Jeonju, Korea.
Korean J Fam Med. 2018 Jan;39(1):54-56. doi: 10.4082/kjfm.2018.39.1.54. Epub 2018 Jan 23.
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.
一小部分人存在中枢性性早熟(CPP)这种神经学异常情况。CPP常见的神经学病因包括肿瘤或先天性病变。虽然阿诺德-奇阿利畸形可由先天性或后天性原因引起,但在CPP患者中并不常见。我们报告一例4.5岁女童,她主诉乳房发育。其神经学检查和生长模式正常。除真性性早熟外,她没有内分泌异常。我们进行了脑部磁共振成像检查,结果显示为1型阿诺德-奇阿利畸形。目前,该病例是表现出1型阿诺德-奇阿利畸形和性早熟的最年幼女童。此外,在该病例中脑病变与性早熟之间很可能存在有意义的关联。