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Pituitary stalk interruption syndrome: A case report

Pituitary stalk interruption syndrome (PSIS) is a rare congenital abnormality. It comprises the triad of thin or interrupted pituitary stalk, aplasia or hypoplasia of anterior pituitary gland, and absent or ectopic posterior pituitary gland. The patient usually presents with a spectrum of symptoms p...

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Detalles Bibliográficos
Autores principales: Dawadi, Kapil, Dahal, Prajwal, Poudyal, Binuda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568276/
https://www.ncbi.nlm.nih.gov/pubmed/37840890
http://dx.doi.org/10.1016/j.radcr.2023.09.010
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author Dawadi, Kapil
Dahal, Prajwal
Poudyal, Binuda
author_facet Dawadi, Kapil
Dahal, Prajwal
Poudyal, Binuda
author_sort Dawadi, Kapil
collection PubMed
description Pituitary stalk interruption syndrome (PSIS) is a rare congenital abnormality. It comprises the triad of thin or interrupted pituitary stalk, aplasia or hypoplasia of anterior pituitary gland, and absent or ectopic posterior pituitary gland. The patient usually presents with a spectrum of symptoms predominantly secondary to anterior pituitary hormonal deficiency. The etiology of this syndrome is not well-established but the genetic cause is considered to be the most common etiology. Early diagnosis is crucial in preventing and reducing morbidity. The prognosis is good if the condition is diagnosed early and the hormonal therapy is started promptly. The diagnosis of PSIS is primarily based on magnetic resonance imaging (MRI) findings.
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spelling pubmed-105682762023-10-13 Pituitary stalk interruption syndrome: A case report Dawadi, Kapil Dahal, Prajwal Poudyal, Binuda Radiol Case Rep Case Report Pituitary stalk interruption syndrome (PSIS) is a rare congenital abnormality. It comprises the triad of thin or interrupted pituitary stalk, aplasia or hypoplasia of anterior pituitary gland, and absent or ectopic posterior pituitary gland. The patient usually presents with a spectrum of symptoms predominantly secondary to anterior pituitary hormonal deficiency. The etiology of this syndrome is not well-established but the genetic cause is considered to be the most common etiology. Early diagnosis is crucial in preventing and reducing morbidity. The prognosis is good if the condition is diagnosed early and the hormonal therapy is started promptly. The diagnosis of PSIS is primarily based on magnetic resonance imaging (MRI) findings. Elsevier 2023-10-03 /pmc/articles/PMC10568276/ /pubmed/37840890 http://dx.doi.org/10.1016/j.radcr.2023.09.010 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Dawadi, Kapil
Dahal, Prajwal
Poudyal, Binuda
Pituitary stalk interruption syndrome: A case report
title Pituitary stalk interruption syndrome: A case report
title_full Pituitary stalk interruption syndrome: A case report
title_fullStr Pituitary stalk interruption syndrome: A case report
title_full_unstemmed Pituitary stalk interruption syndrome: A case report
title_short Pituitary stalk interruption syndrome: A case report
title_sort pituitary stalk interruption syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568276/
https://www.ncbi.nlm.nih.gov/pubmed/37840890
http://dx.doi.org/10.1016/j.radcr.2023.09.010
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