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Atypical Presentation of Panhypopituitarism
Harpreet K Rai1, Geevarghese John1, Maria Anton2
1Internal Medicine, Northwell Health Long Island Jewish Forest Hills Hospital, Forest Hills, USA.
Cureus
|August 14, 2020
Summary
A 59-year-old man with syncope was diagnosed with panhypopituitarism. This rare condition, a deficiency of pituitary hormones, was caused by a pituitary macroadenoma.
Area of Science:
- Endocrinology
- Neurology
Background:
- Hypopituitarism is a rare endocrine disorder involving deficiencies of anterior or posterior pituitary hormones.
- It can manifest as isolated hormone deficiencies or panhypopituitarism, affecting all pituitary hormones.
Observation:
- A 59-year-old man presented with syncope and persistent hypotension despite hydration.
- Initial investigations revealed a sellar mass with calcifications and suprasellar extensions on CT and MRI.
- Differential diagnoses included sepsis, stroke, cardiac arrhythmias, and pulmonary embolism, which were ruled out.
Findings:
- The patient exhibited a deficiency of all anterior pituitary hormones.
- The pituitary macroadenoma was identified as the cause of the mass effect leading to panhypopituitarism.
Implications:
- This case highlights the importance of considering endocrine disorders in patients with unexplained syncope and hypotension.
- Pituitary macroadenomas can present with diverse symptoms, including hormonal deficiencies and neurological effects.
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