Evidence map›Paper›PMID 40841921›Full record

ArticleJournal of medical case reports2025

A case of adrenal insufficiency presenting with seizures, complicated by developmental cerebral venous anomaly and Takotsubo cardiomyopathy: a case report.

Katrina Villegas, Brittany Eason, Karolina Janiec, Alaa Musallam, Ahmed Hammouda, Samia Ammar Aldwaik, Radhika Tailor

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Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Katrina VillegasDepartment of Internal Medicine, St. Joseph's University Medical Center, 703 Main St, Paterson, NJ, USA. katrinajvillegas@gmail.com.ORCID http://orcid.org/0009-0004-9191-3880
Brittany EasonRowan-Virtua School of Osteopathic Medicine, Stratford, NJ, USA.
Karolina JaniecDepartment of Internal Medicine, St. Joseph's University Medical Center, 703 Main St, Paterson, NJ, USA.
Alaa MusallamDepartment of Internal Medicine, St. Joseph's University Medical Center, 703 Main St, Paterson, NJ, USA.
Ahmed HammoudaDepartment of Internal Medicine, St. Joseph's University Medical Center, 703 Main St, Paterson, NJ, USA.
Samia Ammar AldwaikFaculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.
Radhika TailorDepartment of Internal Medicine, St. Joseph's University Medical Center, 703 Main St, Paterson, NJ, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdrenal insufficiency is a potentially life-threatening condition that often presents with nonspecific symptoms. While fatigue, hypotension, and electrolyte disturbances are common features, seizures and stress-induced cardiomyopathy are rare initial manifestations. This case is reported for its atypical presentation and to highlight the diagnostic challenge it posed in the absence of classic biochemical findings. CASE PRESENTATION: We report a case of a 68-year-old Hispanic woman with diabetes, hypertension, dyslipidemia, and hypopituitarism secondary to Sheehan syndrome, who presented with new-onset seizures after abruptly discontinuing chronic steroid therapy. Her symptoms included progressive weakness and behavioral changes over several weeks. Initial evaluation revealed hyperglycemia, mild hyponatremia, and no hyperkalemia-findings consistent with secondary adrenal insufficiency-associated seizures, although contributing to initial diagnostic uncertainty. Brain imaging incidentally identified a developmental cerebral venous anomaly, which was initially suspected as a potential cause of the seizures. In addition, echocardiographic findings were consistent with Takotsubo cardiomyopathy, likely precipitated by the stress of her medical condition. However, further evaluation confirmed adrenal insufficiency with low cortisol and adrenocorticotropic hormone levels, and subnormal response to cosyntropin stimulation. Management included hydrocortisone for adrenal insufficiency and levetiracetam for seizure prophylaxis, leading to symptom resolution and no recurrence of seizures.

conclusionThis case emphasizes the importance of maintaining a high index of suspicion for adrenal insufficiency in patients with a suggestive history, even when classic electrolyte abnormalities are absent and neuroimaging reveals confounding findings. Recognizing rare presentations such as seizures and stress cardiomyopathy can prevent delays in diagnosis and improve outcomes.

Indexed as

Adrenal InsufficiencySeizuresTakotsubo CardiomyopathyAgedAnticonvulsantsEchocardiographyFemaleHumansHydrocortisoneLevetiracetamAnticonvulsantsHydrocortisoneLevetiracetamAdrenal insufficiencyCorticosteroid withdrawalDevelopmental venous anomalySeizuresTakotsubo cardiomyopathy

Identifiers

PMID40841921
PMCPMC12372403

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.