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Asymptomatic Empty Sella Syndrome: A "New" Hypothalamic Pathology or Paraphysiological Variant
Benedetta Masserini1, Benedetta Rivolta1, Irene Bernardi2
1Dirigente Medico, SC Nutrizione Clinica, Diabetologia e Malattie Endocrine, ASST Pavia, Italy.
This case study explores an asymptomatic empty sella syndrome in a 67-year-old female. Despite a decade of untreated pituitary hormone deficiencies, she remained asymptomatic, highlighting a rare presentation of this condition.
Area of Science:
- Endocrinology
- Neuroimaging
- Radiology
Background:
- Empty sella refers to a pituitary gland that is shrunken or displaced.
- It can be primary (genetic) or secondary (trauma, surgery, radiation).
- While 50% of patients are asymptomatic, others experience symptoms like headaches or visual defects.
Purpose of the Study:
- To examine a rare case of asymptomatic empty sella syndrome.
- To discuss the diagnostic and therapeutic challenges associated with this condition.
Main Methods:
- A 67-year-old female patient with dilatative cardiomyopathy was evaluated.
- Magnetic resonance imaging (MRI) confirmed an empty sella.
- Blood tests revealed hypothyroidism, hypoadrenalism, and growth hormone (GH) deficiency.
Main Results:
- The patient had a known history of hormone deficiencies for over a decade without symptoms or complications.
- Despite stress and vascular procedures, she did not experience adrenal crisis or severe hypothyroidism.
- Hormonal replacement therapy was initiated.
Conclusions:
- Asymptomatic empty sella syndrome is rare, contrasting with typical presentations of hormone deficiency.
- The case suggests a potential hypothalamic dysfunction or a physiological variant.
- Further research is needed to determine optimal treatment strategies.
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