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Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer
Pituitary apoplexy is a potentially fatal clinical condition that results from pituitary infarction due to ischemia or hemorrhage. We present a case of a 53-year-old female patient with a history of recurrent pituitary macroadenoma who presented with headache, blurry vision, nausea, vomiting, and ph...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580572/ https://www.ncbi.nlm.nih.gov/pubmed/37908581 http://dx.doi.org/10.1210/jcemcr/luad069 |
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author | Mastandrea, Katherine Voica, Mihail Tetlay, Maryam Hasan, Farhad |
author_facet | Mastandrea, Katherine Voica, Mihail Tetlay, Maryam Hasan, Farhad |
author_sort | Mastandrea, Katherine |
collection | PubMed |
description | Pituitary apoplexy is a potentially fatal clinical condition that results from pituitary infarction due to ischemia or hemorrhage. We present a case of a 53-year-old female patient with a history of recurrent pituitary macroadenoma who presented with headache, blurry vision, nausea, vomiting, and photophobia after receiving a gonadotropin-releasing hormone (GnRH) agonist, leuprolide, as part of adjuvant endocrine therapy for breast cancer. Magnetic resonance imaging (MRI) confirmed the presence of pituitary apoplexy, and endocrine workup showed anterior hypopituitarism. The patient was managed conservatively and required glucocorticoid replacement. A repeat MRI after 3 months showed a partially empty sella. A review of the literature revealed that this case adds to the growing number of patients who present with headache, visual symptoms, and symptoms related to meningeal irritation after administration of GnRH agonists, with varying latency from treatment to symptom onset. Although there are other cases involving female patients or patients with known pituitary macroadenomas, to our knowledge, this is the first reported case of pituitary apoplexy in a patient receiving a GnRH agonist as an adjuvant for breast cancer. Physicians should be aware of this rare complication of GnRH agonist therapy in patients with a pituitary macroadenoma. |
format | Online Article Text |
id | pubmed-10580572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105805722023-10-31 Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer Mastandrea, Katherine Voica, Mihail Tetlay, Maryam Hasan, Farhad JCEM Case Rep Case Report Pituitary apoplexy is a potentially fatal clinical condition that results from pituitary infarction due to ischemia or hemorrhage. We present a case of a 53-year-old female patient with a history of recurrent pituitary macroadenoma who presented with headache, blurry vision, nausea, vomiting, and photophobia after receiving a gonadotropin-releasing hormone (GnRH) agonist, leuprolide, as part of adjuvant endocrine therapy for breast cancer. Magnetic resonance imaging (MRI) confirmed the presence of pituitary apoplexy, and endocrine workup showed anterior hypopituitarism. The patient was managed conservatively and required glucocorticoid replacement. A repeat MRI after 3 months showed a partially empty sella. A review of the literature revealed that this case adds to the growing number of patients who present with headache, visual symptoms, and symptoms related to meningeal irritation after administration of GnRH agonists, with varying latency from treatment to symptom onset. Although there are other cases involving female patients or patients with known pituitary macroadenomas, to our knowledge, this is the first reported case of pituitary apoplexy in a patient receiving a GnRH agonist as an adjuvant for breast cancer. Physicians should be aware of this rare complication of GnRH agonist therapy in patients with a pituitary macroadenoma. Oxford University Press 2023-06-28 /pmc/articles/PMC10580572/ /pubmed/37908581 http://dx.doi.org/10.1210/jcemcr/luad069 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Mastandrea, Katherine Voica, Mihail Tetlay, Maryam Hasan, Farhad Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer |
title | Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer |
title_full | Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer |
title_fullStr | Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer |
title_full_unstemmed | Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer |
title_short | Pituitary Apoplexy Secondary to Gonadotropin-Releasing Hormone Agonist for Breast Cancer |
title_sort | pituitary apoplexy secondary to gonadotropin-releasing hormone agonist for breast cancer |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580572/ https://www.ncbi.nlm.nih.gov/pubmed/37908581 http://dx.doi.org/10.1210/jcemcr/luad069 |
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