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The pituitary stalk transection syndrome: multifaceted presentation in adulthood
Adriana Gabriela Ioachimescu1, Amir H Hamrahian, Mariam Stevens
1Department of Medicine and Neurological Surgery, Emory University School of Medicine, 1365 B Clifton Rd NE, Atlanta, GA 30322, USA. aioachi@emory.edu
Pituitary stalk transection syndrome, identified by MRI, presents varied hormonal deficits throughout life. Adult endocrinologists must consider this condition for patients with unexplained pituitary issues.
Area of Science:
- Endocrinology
- Radiology
- Pediatric Endocrinology
Background:
- Pituitary stalk transection syndrome (PSTS) is often diagnosed in childhood but its adult prevalence and natural history remain unclear.
- Magnetic Resonance Imaging (MRI) has been crucial in characterizing PSTS, revealing specific anatomical abnormalities.
Observation:
- This study details four adult cases of PSTS, highlighting its diverse clinical manifestations.
- All patients exhibited characteristic MRI findings: a small anterior pituitary, absent or diminutive infundibulum, and ectopic posterior pituitary.
- Hormonal deficiencies varied in onset and severity, with adrenal insufficiency, growth hormone deficiency, hypothyroidism, and hypogonadism observed across different ages.
Findings:
- PSTS can present with pleiotropic manifestations and variable hormonal deficits, including adrenal insufficiency, growth hormone deficiency, hypothyroidism, and hypogonadism.
- The syndrome's onset can range from childhood to the second decade of life, with deficiencies potentially emerging later.
- Characteristic MRI findings are key to diagnosing PSTS.
Implications:
- PSTS should be considered in adults with previously diagnosed idiopathic growth hormone deficiency or multiple pituitary hormone deficiencies.
- MRI findings suggestive of PSTS warrant a comprehensive hormonal evaluation.
- Long-term endocrinological follow-up is essential for adult patients with PSTS due to the potential for new hormone deficiencies to develop over time.
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