Gonadotropin Suppression for 7 Years After a Single Histrelin Implant for Precocious Puberty.

bone age delay central precocious puberty gonadotropin-releasing hormone analogue gynecomastia

Journal

Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997

Informations de publication

Date de publication:
01 Feb 2022
Historique:
received: 12 10 2021
entrez: 20 1 2022
pubmed: 21 1 2022
medline: 21 1 2022
Statut: epublish

Résumé

Gonadotropin-releasing hormone analogues (GnRHas) are an effective treatment to address the compromise in height potential seen in patients with central precocious puberty. There is no evidence in the literature of a single GnRHa used for longer than 2 years before being removed or replaced. We describe a patient who was on continuous gonadotropin suppression for 7 years and despite this, achieved a height potential within 1 SD of mid-parental height. A boy aged 10 years 3 months presented to the endocrine clinic with signs of precocious puberty and advanced bone age. Initial laboratory values were a random luteinizing hormone (LH) level of 9.4 mIU/mL, follicle-stimulating hormone (FSH) 16.3 mIU/mL, dehydroepiandrosterone sulfate 127 mcg/dL, and testosterone 628 ng/dL. The patient was initially started on Lupron injections before transitioning to a histrelin implant. Follow-up laboratory results 5 months post-suppression showed pre-pubertal random LH 0.2 mIU/mL, FSH 0.1 mIU/mL, and testosterone 5 ng/dL. The patient was lost to follow-up and returned 5 years later presenting with gynecomastia and delayed bone age. He had continuous gonadotropin suppression with random LH 0.10 mIU/mL, FSH 0.16 mIU/mL, and testosterone 8 ng/dL. The histrelin implant was removed, and 4 months later, his random pubertal hormone levels were LH 5.6 mIU/mL, FSH 4.3 mIU/mL, and testosterone 506 ng/dL. The patient's mid-parental height was 175.3 cm and his near final height was 170.6 cm, which is within 1 SD of his genetic potential. Further studies are needed to explore continuous gonadotropin hormone suppression with a single histrelin implant beyond 2 years.

Identifiants

pubmed: 35047716
doi: 10.1210/jendso/bvab189
pii: bvab189
pmc: PMC8758400
doi:

Types de publication

Case Reports

Langues

eng

Pagination

bvab189

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society.

Références

Paediatr Drugs. 2015 Aug;17(4):273-81
pubmed: 25911294
J Clin Endocrinol Metab. 2015 Jun;100(6):2354-63
pubmed: 25803268
Andrology. 2019 Nov;7(6):778-793
pubmed: 31099174
Int J Pediatr Endocrinol. 2009;2009:812517
pubmed: 19956699
Eur J Endocrinol. 2017 Jun;176(6):R339-R353
pubmed: 28274950
Pediatrics. 2005 Dec;116(6):e798-802
pubmed: 16322137
N Engl J Med. 2007 Sep 20;357(12):1229-37
pubmed: 17881754
J Pediatr. 2014 Apr;164(4):912-916.e1
pubmed: 24433825
J Pediatr. 2013 Oct;163(4):1214-6
pubmed: 23809043

Auteurs

Douglas Villalta (D)

The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.

Jose B Quintos (JB)

Division of Pediatric Endocrinology, Rhode Island Hospital/Hasbro Children's Hospital-The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.

Classifications MeSH