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A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis
BACKGROUND: Pituitary apoplexy (PA) is a clinical syndrome of pituitary hemorrhage or infarction and can result in hypopituitarism as well as compression of adjacent brain structures. Visual loss occurs frequently, as a result of tumor expansion and compression of the optic chiasm and optic nerves....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154637/ https://www.ncbi.nlm.nih.gov/pubmed/37152694 http://dx.doi.org/10.1155/2023/3183088 |
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author | Jamal, Yusra Camacho, Yudi Hanft, Simon Chiarolanzio, Patrick Goldberg, Michael D. Mullally, Jamie A. |
author_facet | Jamal, Yusra Camacho, Yudi Hanft, Simon Chiarolanzio, Patrick Goldberg, Michael D. Mullally, Jamie A. |
author_sort | Jamal, Yusra |
collection | PubMed |
description | BACKGROUND: Pituitary apoplexy (PA) is a clinical syndrome of pituitary hemorrhage or infarction and can result in hypopituitarism as well as compression of adjacent brain structures. Visual loss occurs frequently, as a result of tumor expansion and compression of the optic chiasm and optic nerves. Additionally, with pituitary tumor invasion into the fixed space of the cavernous sinus, compression of multiple cranial nerves can result in cavernous sinus syndrome (CSS). We describe a case of an undiagnosed pituitary tumor manifesting as abrupt PA with CSS during hemodialysis (HD). Clinical Case. A 77-year-old male with end-stage renal disease (ESRD) presented with acute onset of severe headache, decreased vision, ophthalmoplegia of the left eye, and hypotension during HD. MRI of the brain revealed a 2.5 cm pituitary adenoma with acute hemorrhage, compression of the left prechiasmatic optic nerve, and invasion into the left cavernous sinus (CS). The hormonal profile was consistent with multiple pituitary hormone deficiencies. The patient was treated with glucocorticoids and underwent transsphenoidal resection of the tumor. He had an uneventful postoperative hospital course, and his left visual acuity stabilized, although there was no immediate improvement in his other ocular symptoms. CONCLUSION: Our case highlights a rare constellation of a pituitary adenoma with CS invasion complicated by PA and CSS during HD. The pathophysiology of PA is not well understood, and there are very limited data regarding PA in patients with end-stage renal disease (ESRD) on HD. Prompt recognition of PA in a patient presenting with CSS, particularly in the HD setting, is essential to ensure appropriate care is provided for this medical emergency. |
format | Online Article Text |
id | pubmed-10154637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-101546372023-05-04 A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis Jamal, Yusra Camacho, Yudi Hanft, Simon Chiarolanzio, Patrick Goldberg, Michael D. Mullally, Jamie A. Case Rep Endocrinol Case Report BACKGROUND: Pituitary apoplexy (PA) is a clinical syndrome of pituitary hemorrhage or infarction and can result in hypopituitarism as well as compression of adjacent brain structures. Visual loss occurs frequently, as a result of tumor expansion and compression of the optic chiasm and optic nerves. Additionally, with pituitary tumor invasion into the fixed space of the cavernous sinus, compression of multiple cranial nerves can result in cavernous sinus syndrome (CSS). We describe a case of an undiagnosed pituitary tumor manifesting as abrupt PA with CSS during hemodialysis (HD). Clinical Case. A 77-year-old male with end-stage renal disease (ESRD) presented with acute onset of severe headache, decreased vision, ophthalmoplegia of the left eye, and hypotension during HD. MRI of the brain revealed a 2.5 cm pituitary adenoma with acute hemorrhage, compression of the left prechiasmatic optic nerve, and invasion into the left cavernous sinus (CS). The hormonal profile was consistent with multiple pituitary hormone deficiencies. The patient was treated with glucocorticoids and underwent transsphenoidal resection of the tumor. He had an uneventful postoperative hospital course, and his left visual acuity stabilized, although there was no immediate improvement in his other ocular symptoms. CONCLUSION: Our case highlights a rare constellation of a pituitary adenoma with CS invasion complicated by PA and CSS during HD. The pathophysiology of PA is not well understood, and there are very limited data regarding PA in patients with end-stage renal disease (ESRD) on HD. Prompt recognition of PA in a patient presenting with CSS, particularly in the HD setting, is essential to ensure appropriate care is provided for this medical emergency. Hindawi 2023-04-25 /pmc/articles/PMC10154637/ /pubmed/37152694 http://dx.doi.org/10.1155/2023/3183088 Text en Copyright © 2023 Yusra Jamal et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Jamal, Yusra Camacho, Yudi Hanft, Simon Chiarolanzio, Patrick Goldberg, Michael D. Mullally, Jamie A. A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis |
title | A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis |
title_full | A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis |
title_fullStr | A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis |
title_full_unstemmed | A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis |
title_short | A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis |
title_sort | case of pituitary apoplexy and cavernous sinus syndrome during hemodialysis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154637/ https://www.ncbi.nlm.nih.gov/pubmed/37152694 http://dx.doi.org/10.1155/2023/3183088 |
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