Pituitary apoplexy with acute complete bilateral third nerve palsy and papillary involvement: A case report

Author:

Bahadoram M.1ORCID,Sadrian M.1ORCID,Sharififard M.1ORCID,Akade E.1ORCID,Rasras S.1ORCID

Affiliation:

1. Ahvaz Jundishapur University of Medical Sciences

Abstract

   Pituitary apoplexy (PA) is a rare, potentially life-threatening condition primarily associated with pituitary adenomas. It presents with sudden, severe symptoms due to inadequate blood supply, bleeding, or tissue death in the pituitary gland. This case report describes a case of PA in a 40-year-old female, and reviews the recent literature surrounding the subject. The patient presented with complete bilateral third nerve palsy and dilated non-reactive pupils. Her initial symptoms included retroorbital headache, fever, and double vision, which rapidly progressed to oculomotor nerve palsy. MRI revealed hemorrhagic PA. High-dose steroids were initiated, leading to the resolution of ptosis. Additionally, surgical intervention was performed. PA typically affects older males with known adenomas, making this case unusual due to the patient's age, gender, and absence of prior adenoma history. Differentiating PA from other intracranial pathologies is crucial, and MRI plays a pivotal role in accurate diagnosis.

Publisher

IMA Press, LLC

Reference16 articles.

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3. Shrestha R, Bishokarma S, Rayamajhi S, et al. Pituitary apoplexy presenting as isolated third cranial nerve palsy: case series. J Surg Case Rep. 2022 Aug 23;2022(8):rjac386. doi: 10.1093/jscr/rjac386

4. Tupputi U, Testini V, Manco MGR, et al. Two rare cases of pituitary apoplexy in adult females: a tricky diagnosis [JB]. Acta Biomed Atenei Parmensis. 2023;94(S1):e2023029. doi: 10.23750/abm.v94iS1.13531

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