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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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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. |
format | Online Article Text |
id | pubmed-10562649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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