Pituitary stalk interruption syndrome: a case report and literature review

Author:

Ali Alqarni Abdullah1,Abdalla Khalid Mohamed2,Alqarni Mohammed A. S.3,Alfaifi Jaber A.4,Osman Hisham G. A.2,Al Alhindi Bandar S.1

Affiliation:

1. Department of Medicine, College of Medicine, University of Bisha

2. King Abdullah Hospital, Bisha, Kingdom of Saudi Arabia

3. Hospital Director of Maternity and Children’s Hospital

4. Department of Child Health, College of Medicine, University of Bisha

Abstract

Background: Pituitary stalk interruption syndrome is a rare congenital anomaly of the pituitary gland characterized by growth hormones deficiency (with or without other pituitary hormone deficiencies) along with radiological features of a thin or interrupted pituitary stalk, an ectopic or absent posterior pituitary, or a hypoplastic or absent anterior pituitary. Case presentation: A 10-year-old baby boy came with short stature. The laboratory investigations were done and showed low growth hormones and low thyroid-stimulating hormone. MRI showed an ectopic posterior pituitary, a small hypoplastic anterior pituitary, and an absent pituitary stalk. Conclusion: Pituitary stalk interruption syndrome is a very rare entity. MRI is used to diagnose it. Early detection of this syndrome improve the patient symptoms especially before puberty.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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