An unrecognized endocrinology emergency masquerading as a hypertensive emergency: A can’t miss diagnosis

Yanerys Agosto Vargas, Sharon Velez Maymi, Paola Mansilla Letelier, Luis Raul Hernandez-Vazquez, Samayra Miranda Rodriguez, Michelle Mangual Garcia, Jose Rodriguez Leon, José H. Martínez, Madeleine Gutierrez, Maria de Lourdes Miranda

Abstract


Pituitary apoplexy secondary to sellar tumors is a rare entity that carries a high mortality rate. It could be secondary to infarction or hemorrhage of the pituitary gland. The incidence remains unclear, most are reported in men between the ages of 50 to 60. In the majority of times, apoplexy is idiopathic in nature, without a clear discernible cause. However, there are multiple risk factors associated with this entity, such as systemic hypertension, among others. There are few cases of pituitary apoplexy caused by infarction of a pituitary macroadenoma. We present this case of pituitary apoplexy secondary to infarction of a nonfunctional pituitary adenoma in a young woman, with a fortunate resolution.


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DOI: https://doi.org/10.5430/crim.v4n1p21

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Case Reports in Internal Medicine

ISSN 2332-7243(Print)  ISSN 2332-7251(Online)

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