# Hyperosmolar Hyperglycemic State With Reversible Encephalopathy in a Young Female on Chronic Steroids and Opioids: A Case Report

**Authors:** Athena Myrou

PMC · DOI: 10.7759/cureus.99304 · Cureus · 2025-12-15

## TL;DR

A young woman on long-term steroids and opioids developed a rare hyperglycemic condition with brain symptoms, highlighting the risk in atypical populations.

## Contribution

This case report presents HHS with reversible encephalopathy in a young adult with chronic steroid and opioid use, a rare clinical scenario.

## Key findings

- The patient exhibited severe hyperglycemia and encephalopathy despite being young and having no typical diabetes history.
- Neuroimaging ruled out acute intracranial pathology, and the patient fully recovered with fluid and insulin therapy.
- Chronic steroid use suppressed the HPA axis, and opioid exposure may have contributed to the metabolic crisis.

## Abstract

Hyperosmolar hyperglycemic state (HHS) is uncommon in young adults and may signal complex metabolic and pharmacologic interactions, particularly in the context of chronic glucocorticoid and opioid exposure. We describe a 22-year-old female with morbid obesity, idiopathic intracranial hypertension treated with ventriculoperitoneal shunting and neuromodulation, chronic high-dose steroid use, and opioid exposure who presented with severe hyperglycemia, dehydration, headache, and transient confusion. Laboratory findings revealed glucose level of 583 mg/dL, calculated osmolality of approximately 318 mOsm/kg, preserved C-peptide indicating severe insulin resistance, and suppressed adrenocorticotropic hormone and cortisol consistent with exogenous steroid-induced hypothalamic-pituitary-adrenal axis suppression. Urine ketones were present, but serum ketones were absent, supporting HHS without ketoacidosis. Neuroimaging excluded acute intracranial pathology. The patient improved with intravenous fluids, insulin therapy, treatment of intercurrent infection, and careful steroid tapering, achieving full neurologic recovery. This case highlights the potential for hyperosmolar neuro-metabolic crisis in young adults with chronic steroid and opioid exposure and emphasizes the importance of considering HHS in atypical populations, particularly when obesity, prolonged glucocorticoid therapy, and central nervous system depressants coexist.

## Linked entities

- **Chemicals:** opioid (PubChem CID 126961754)
- **Diseases:** idiopathic intracranial hypertension (MONDO:0009468), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}
- **Diseases:** dehydration (MESH:D003681), headache (MESH:D006261), insulin resistance (MESH:D007333), neuro-metabolic crisis (MESH:D008659), HHS (MESH:D006944), Encephalopathy (MESH:D001927), hyperglycemia (MESH:D006943), infection (MESH:D007239), confusion (MESH:D003221), obesity (MESH:D009765), intracranial hypertension (MESH:D019586), ketoacidosis (MESH:D007662)
- **Chemicals:** Steroids (MESH:D013256), C-peptide (MESH:D002096), glucose (MESH:D005947), cortisol (MESH:D006854), ketones (MESH:D007659)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12803434/full.md

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Source: https://tomesphere.com/paper/PMC12803434