Precocious puberty in McCune-Albright syndrome: a case report
Penulis/Author
RIANTI PUJI LESTARI (1); Prof. dr. Retno Sutomo, Sp.A(K)., Ph.D. (2); Prof. dr. Madarina Julia, Sp.A(K), MPH., Ph.D. (3)
Tanggal/Date
2018
Kata Kunci/Keyword
Abstrak/Abstract
McCune-Albright syndrome (MAS) is a rare disease characterized by a triad of fibrous dysplasia, cafe-au-lait spots and peripheral precocious puberty. We reported a 5-year-8-month old girl with MAS who has been followed-up for 2 years and 8 months. She was referred to pediatric endocrinology clinic in our hospital for vaginal bleeding at age of 2 years 11 months. She had peripheral precocious puberty, ie increased estrogen level associated with very low gonadotropins, and cafe-au-lait spots on her face and was diagnosed as MAS. The patient was treated with estrogen receptor blocker (tamoxifen). She had no menses during the 2 years and 8 months of tamoxifen treatment. Her growth rate and bone maturation were also in normal ranges. However, at the end of tamoxifen treatment she had an episode of vaginal bleeding so that we had to change to other treatment modalities.
Rumpun Ilmu
Penyakit Anak
Bahasa Asli/Original Language
English
Level
Nasional
Status
Dokumen Karya
No
Judul
Tipe Dokumen
Aksi
1
2018 Precocious puberty in McCune-Albright syndrome- a case report .pdf
Bukti Published
2
2018_JMedSci_Precocious puberty in McCune-Albright.pdf
[PAK] Full Dokumen
3
Akreditasi JMedSci BIK.pdf
4
MJ tanpa EC paper Rianti.pdf
Dokumen Pendukung Karya Ilmiah (Hibah, Publikasi, Penelitian, Pengabdian)