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Pituitary Stalk Interruption Syndrome: A Case Report

Pituitary stalk interruption syndrome is a congenital abnormality. The triad of this syndrome comprises a thin pituitary stalk, an ectopic posterior pituitary gland, and an absent or hypoplastic anterior pituitary gland. The patient typically presents with a spectrum of symptoms secondary to anterio...

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Autores principales: Ziad, Alishbah, Khan, Quratulain, Farooq, Hira, Rehman, Anis, Siddique, Kashif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650926/
https://www.ncbi.nlm.nih.gov/pubmed/36381694
http://dx.doi.org/10.7759/cureus.30218
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author Ziad, Alishbah
Khan, Quratulain
Farooq, Hira
Rehman, Anis
Siddique, Kashif
author_facet Ziad, Alishbah
Khan, Quratulain
Farooq, Hira
Rehman, Anis
Siddique, Kashif
author_sort Ziad, Alishbah
collection PubMed
description Pituitary stalk interruption syndrome is a congenital abnormality. The triad of this syndrome comprises a thin pituitary stalk, an ectopic posterior pituitary gland, and an absent or hypoplastic anterior pituitary gland. The patient typically presents with a spectrum of symptoms secondary to anterior pituitary hormonal deficiency. The etiology of this syndrome is not established but is likely due to a genetic mutation. The prognosis is good if the syndrome is diagnosed early and hormonal therapy is started promptly. Early diagnosis is crucial in preventing adverse effects on growth and development. The diagnosis of pituitary stalk interruption syndrome is based on magnetic resonance imaging (MRI) findings. This study presents the case of a young girl who presented with complaints of short stature and amenorrhea and was diagnosed with pituitary stalk interruption syndrome following an MRI.
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spelling pubmed-96509262022-11-14 Pituitary Stalk Interruption Syndrome: A Case Report Ziad, Alishbah Khan, Quratulain Farooq, Hira Rehman, Anis Siddique, Kashif Cureus Endocrinology/Diabetes/Metabolism Pituitary stalk interruption syndrome is a congenital abnormality. The triad of this syndrome comprises a thin pituitary stalk, an ectopic posterior pituitary gland, and an absent or hypoplastic anterior pituitary gland. The patient typically presents with a spectrum of symptoms secondary to anterior pituitary hormonal deficiency. The etiology of this syndrome is not established but is likely due to a genetic mutation. The prognosis is good if the syndrome is diagnosed early and hormonal therapy is started promptly. Early diagnosis is crucial in preventing adverse effects on growth and development. The diagnosis of pituitary stalk interruption syndrome is based on magnetic resonance imaging (MRI) findings. This study presents the case of a young girl who presented with complaints of short stature and amenorrhea and was diagnosed with pituitary stalk interruption syndrome following an MRI. Cureus 2022-10-12 /pmc/articles/PMC9650926/ /pubmed/36381694 http://dx.doi.org/10.7759/cureus.30218 Text en Copyright © 2022, Ziad et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Endocrinology/Diabetes/Metabolism
Ziad, Alishbah
Khan, Quratulain
Farooq, Hira
Rehman, Anis
Siddique, Kashif
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 Endocrinology/Diabetes/Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650926/
https://www.ncbi.nlm.nih.gov/pubmed/36381694
http://dx.doi.org/10.7759/cureus.30218
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