Successful pregnancies and deliveries in a patient with evolving hypopituitarism due to pituitary stalk transection syndrome: Role of growth hormone replacement

7Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.

Abstract

We herein report a 31-year-old Japanese woman with evolving hypopituitarism due to pituitary stalk transection syndrome. She had a history of short stature treated with growth hormone (GH) in childhood and had hypothyroidism and primary amenorrhea at 20 years old. Levothyroxine replacement and recombinant follicle stimulating hormone-human chorionic gonadotropin (FSH-hCG) therapy for ovulation induction were started. GH replacement therapy (GHRT) was resumed when she was 26 years old. She developed mild adrenocortical insufficiency at 31 years old. She succeeded in becoming pregnant and delivered twice. GHRT was partially continued during pregnancy and stopped at the end of the second trimester without any complications.

Cite

CITATION STYLE

APA

Yoshizawa, M., Ieki, Y., Takazakura, E., Fukuta, K., Hidaka, T., Wakasugi, T., & Shimatsu, A. (2017). Successful pregnancies and deliveries in a patient with evolving hypopituitarism due to pituitary stalk transection syndrome: Role of growth hormone replacement. Internal Medicine, 56(5), 527–530. https://doi.org/10.2169/internalmedicine.56.7478

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free