Pituitary Stalk Interruption Syndrome: A Case and Literature Review

Background/Objective: Pituitary stalk interruption syndrome (PSIS) is a rare congenital disorder that is characterized by a triad including a thin or interrupted pituitary stalk, absent or ectopic posterior lobe, and agenesis or dysgenesis of anterior lobe.PSIS is typically diagnosed in childhood. T...

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Main Authors: Anuja Choure, MD, Leena Shahla, MD
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:AACE Clinical Case Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2376060524001081
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author Anuja Choure, MD
Leena Shahla, MD
author_facet Anuja Choure, MD
Leena Shahla, MD
author_sort Anuja Choure, MD
collection DOAJ
description Background/Objective: Pituitary stalk interruption syndrome (PSIS) is a rare congenital disorder that is characterized by a triad including a thin or interrupted pituitary stalk, absent or ectopic posterior lobe, and agenesis or dysgenesis of anterior lobe.PSIS is typically diagnosed in childhood. The objective of this report is to describe a patient with PSIS whose diagnosis was missed until adulthood. Case Report: A 42-year-old-female presented for evaluation of premature menopause, weight loss, and occasional dizziness. On examination she had short stature and absent secondary sexual features. Laboratory tests were consistent with hypopituitarism with follicle stimulating hormone 0.5 mIU/mL (16.7-113); luteinizing hormone 1.2 mIU/mL (10.8-58.6); prolactin 10.4 ng/mL (2.7-19.6); estradiol 20 pg/mL; cortisol 2 mcg/dL (6.7-22.6); adrenocorticotropic hormone 18 pg/mL (6-50); thyroid stimulating hormone 10.33 uIU/mL (0.28-3.8); free T4 0.41 ng/dL (0.58-1.64); insulin like growth factor-1 −3.7 SD (17 ng/mL) (52-328); and adrenocorticotropic hormone stimulation confirmed secondary adrenal insufficiency. The magnetic resonance imaging of the brain revealed an ectopic posterior pituitary with a partially empty sella, absence of the pituitary stalk, and a small anterior pituitary. The patient was initiated on replacement hormones with improvement in her symptoms. Discussion: PSIS is a rare condition with uncertain pathogenesis and variable presentation requiring a high index of suspicion and presenting with multiple anterior pituitary hormone deficiencies. Diagnosis is confirmed by a dedicated pituitary magnetic resonance imaging, and treatment is tailored to the hormonal deficiency detected. Conclusion: This case highlights the importance of early diagnosis of PSIS, which presents with multiple anterior pituitary hormonal deficiencies, but diagnosis can remain elusive unless dedicated brain imaging is performed.
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spelling doaj-art-3b3434532a7c4328b4e0c211bcbb8af62025-01-15T04:11:44ZengElsevierAACE Clinical Case Reports2376-06052025-01-011112931Pituitary Stalk Interruption Syndrome: A Case and Literature ReviewAnuja Choure, MD0Leena Shahla, MD1Department of Endocrinology, Diabetes & Metabolism, University of Arizona College of Medicine, Phoenix, Arizona; Address correspondence to Dr Anuja Choure, Department of Endocrinology, Diabetes & Metabolism, University of Arizona College of Medicine, 4050 S Emerson St, Phoenix, AZ 85248.Division of Endocrinology, Department of Medicine, Duke University, Durham, North CarolinaBackground/Objective: Pituitary stalk interruption syndrome (PSIS) is a rare congenital disorder that is characterized by a triad including a thin or interrupted pituitary stalk, absent or ectopic posterior lobe, and agenesis or dysgenesis of anterior lobe.PSIS is typically diagnosed in childhood. The objective of this report is to describe a patient with PSIS whose diagnosis was missed until adulthood. Case Report: A 42-year-old-female presented for evaluation of premature menopause, weight loss, and occasional dizziness. On examination she had short stature and absent secondary sexual features. Laboratory tests were consistent with hypopituitarism with follicle stimulating hormone 0.5 mIU/mL (16.7-113); luteinizing hormone 1.2 mIU/mL (10.8-58.6); prolactin 10.4 ng/mL (2.7-19.6); estradiol 20 pg/mL; cortisol 2 mcg/dL (6.7-22.6); adrenocorticotropic hormone 18 pg/mL (6-50); thyroid stimulating hormone 10.33 uIU/mL (0.28-3.8); free T4 0.41 ng/dL (0.58-1.64); insulin like growth factor-1 −3.7 SD (17 ng/mL) (52-328); and adrenocorticotropic hormone stimulation confirmed secondary adrenal insufficiency. The magnetic resonance imaging of the brain revealed an ectopic posterior pituitary with a partially empty sella, absence of the pituitary stalk, and a small anterior pituitary. The patient was initiated on replacement hormones with improvement in her symptoms. Discussion: PSIS is a rare condition with uncertain pathogenesis and variable presentation requiring a high index of suspicion and presenting with multiple anterior pituitary hormone deficiencies. Diagnosis is confirmed by a dedicated pituitary magnetic resonance imaging, and treatment is tailored to the hormonal deficiency detected. Conclusion: This case highlights the importance of early diagnosis of PSIS, which presents with multiple anterior pituitary hormonal deficiencies, but diagnosis can remain elusive unless dedicated brain imaging is performed.http://www.sciencedirect.com/science/article/pii/S2376060524001081ectopic posterior pituitaryinterrupted pituitary stalkPSISshort stature
spellingShingle Anuja Choure, MD
Leena Shahla, MD
Pituitary Stalk Interruption Syndrome: A Case and Literature Review
AACE Clinical Case Reports
ectopic posterior pituitary
interrupted pituitary stalk
PSIS
short stature
title Pituitary Stalk Interruption Syndrome: A Case and Literature Review
title_full Pituitary Stalk Interruption Syndrome: A Case and Literature Review
title_fullStr Pituitary Stalk Interruption Syndrome: A Case and Literature Review
title_full_unstemmed Pituitary Stalk Interruption Syndrome: A Case and Literature Review
title_short Pituitary Stalk Interruption Syndrome: A Case and Literature Review
title_sort pituitary stalk interruption syndrome a case and literature review
topic ectopic posterior pituitary
interrupted pituitary stalk
PSIS
short stature
url http://www.sciencedirect.com/science/article/pii/S2376060524001081
work_keys_str_mv AT anujachouremd pituitarystalkinterruptionsyndromeacaseandliteraturereview
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