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A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature

A 78‐year‐old man was referred to clinic due to a 5‐year history of weight loss, lethargy, and pathology showing hyponatremia. In the year prior, he had a hospital admission for symptomatic hyponatremia. MRI brain during that admission showed a 1–2 mm pituitary lesion of unknown significance. Testin...

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Autores principales: Azam, Hamza, Tuch, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562649/
https://www.ncbi.nlm.nih.gov/pubmed/37822479
http://dx.doi.org/10.1002/ccr3.8026
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author Azam, Hamza
Tuch, Bernard
author_facet Azam, Hamza
Tuch, Bernard
author_sort Azam, Hamza
collection PubMed
description A 78‐year‐old man was referred to clinic due to a 5‐year history of weight loss, lethargy, and pathology showing hyponatremia. In the year prior, he had a hospital admission for symptomatic hyponatremia. MRI brain during that admission showed a 1–2 mm pituitary lesion of unknown significance. Testing during this presentation revealed hypocortisolism with ACTH deficiency. Progress MRI brain revealed the presence of a Rathke's Cleft Cyst (RC). Medical management with glucocorticoids resulted in symptomatic and biochemical parameter improvement. To our knowledge this is the first reported case of isolated ACTH deficiency in the setting of a RC.
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spelling pubmed-105626492023-10-11 A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature Azam, Hamza Tuch, Bernard Clin Case Rep Case Report A 78‐year‐old man was referred to clinic due to a 5‐year history of weight loss, lethargy, and pathology showing hyponatremia. In the year prior, he had a hospital admission for symptomatic hyponatremia. MRI brain during that admission showed a 1–2 mm pituitary lesion of unknown significance. Testing during this presentation revealed hypocortisolism with ACTH deficiency. Progress MRI brain revealed the presence of a Rathke's Cleft Cyst (RC). Medical management with glucocorticoids resulted in symptomatic and biochemical parameter improvement. To our knowledge this is the first reported case of isolated ACTH deficiency in the setting of a RC. John Wiley and Sons Inc. 2023-10-09 /pmc/articles/PMC10562649/ /pubmed/37822479 http://dx.doi.org/10.1002/ccr3.8026 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Azam, Hamza
Tuch, Bernard
A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature
title A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature
title_full A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature
title_fullStr A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature
title_full_unstemmed A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature
title_short A rare case of isolated ACTH deficiency associated with a Rathke's Cleft Cyst and a review of the literature
title_sort rare case of isolated acth deficiency associated with a rathke's cleft cyst and a review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562649/
https://www.ncbi.nlm.nih.gov/pubmed/37822479
http://dx.doi.org/10.1002/ccr3.8026
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