# Paroxysmal Hemidystonia as the Presenting Manifestation of Previously Undiagnosed Diabetes Mellitus

**Authors:** Subhankar Chatterjee, Samya Sengupta, Ritwik Ghosh, Julián Benito-León, Souvik Dubey

PMC · DOI: 10.5334/tohm.1185 · 2026-03-24

## TL;DR

A 72-year-old man with unexplained paroxysmal dystonia was found to have undiagnosed diabetes, showing that dystonia can be a rare early sign of hyperglycemia.

## Contribution

This case expands the known movement disorders associated with hyperglycemia to include paroxysmal hemidystonia as a possible initial sign of diabetes.

## Key findings

- The patient's abnormal movements resolved after correcting hyperglycemia.
- Brain imaging showed no acute striatal lesion, but subtle hypometabolism in the left cerebellum was observed post-recovery.
- The case emphasizes the importance of glucose testing in patients with new-onset paroxysmal hyperkinetic movements.

## Abstract

Hyperglycemia-related movement disorders classically present as hemichorea-hemiballismus, whereas dystonia is far less common and may occasionally precede the recognition of diabetes mellitus.

A 72-year-old man presented with a 3-month history of recurrent, stereotyped dystonic spells involving the right side of the face, arm, and leg. These episodes occurred approximately twice per minute and lasted about 5 seconds each. Initial laboratory testing revealed a plasma glucose level of 494 mg/dL and an HbA1c of 16.1%, consistent with previously unrecognized diabetes mellitus. Electrolyte levels, electroencephalography, cerebrospinal fluid analysis, and evaluation for autoimmune encephalopathy were unremarkable. Brain MRI showed only a chronic lacunar infarct in the left basal ganglia, with no evidence of an acute striatal lesion. The abnormal movements resolved completely within 3 days after correction of hyperglycemia. Follow-up 18F-FDG PET/CT performed after clinical recovery demonstrated subtle relative hypometabolism in the left cerebellum, with preserved uptake in the basal ganglia and cerebral cortex.

This case broadens the phenomenologic spectrum of hyperglycemia-related movement disorders and highlights paroxysmal hemidystonia as a potential presenting manifestation of previously undiagnosed diabetes mellitus. Bedside glucose testing should therefore be routinely performed in the evaluation of new-onset paroxysmal hyperkinetic movements. In addition, isolated extra-striatal metabolic abnormalities detected after symptom resolution should be interpreted with caution.

## Linked entities

- **Diseases:** diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Diseases:** autoimmune encephalopathy (MESH:D001927), movement disorders (MESH:D009069), Paroxysmal Hemidystonia (MESH:D002819), metabolic abnormalities (MESH:D008659), Hyperglycemia (MESH:D006943), dystonic spells (MESH:D004411), abnormal movements (MESH:D004409), dystonia (MESH:D004421), hemichorea-hemiballismus (MESH:D020820), hyperkinetic movements (MESH:D006948), Diabetes Mellitus (MESH:D003920), striatal lesion (MESH:C537500), lacunar infarct (MESH:D059409)
- **Chemicals:** 18F (MESH:C000615276), glucose (MESH:D005947), FDG (MESH:D019788)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13025155/full.md

---
Source: https://tomesphere.com/paper/PMC13025155