# Early diagnostic challenges of isolated ocular motor nerve palsy: diabetic, ischemic, or Tolosa-Hunt Syndrome

**Authors:** Ling Yu, Wei Qin, Wenli Hu, Lei Yang

PMC · DOI: 10.3389/fneur.2025.1592993 · Frontiers in Neurology · 2025-07-17

## TL;DR

The paper studies the early diagnosis of isolated ocular motor nerve palsy, focusing on distinguishing between diabetic, ischemic, and Tolosa-Hunt causes.

## Contribution

It provides insights into clinical and imaging differences between diabetic and non-diabetic patients with this condition.

## Key findings

- 46 out of 68 patients met criteria for microvascular ocular motor nerve palsy.
- 19 patients were diagnosed with Tolosa-Hunt syndrome, with similar pain relief rates in diabetic and non-diabetic groups.
- There is a need for standardized diagnostic criteria due to overlapping features between conditions.

## Abstract

Investigating the clinical features and etiological diagnosis of early isolated ocular motor nerve palsy to deepen understanding of the condition.

We retrospectively enrolled 68 patients with isolated ocular motor nerve palsy admitted our hospital between 2017 and 2024. A retrospective analysis was conducted to assess their clinical and imaging characteristics. Based on current diagnostic criteria, patients were categorized into one of the following groups: diabetic ophthalmoplegia (DO), microvascular ocular motor nerve palsies (MVP), or Tolosa-Hunt syndrome (THS). Patients were divided into two groups based on the presence of diabetes, and the clinical and imaging differences between the two groups were compared.

Of the 68 patients, 40 were male, with an average age of 61 years. There were 43 patients with diabetes, and 40 had a history of hypertension. The number of patients with isolated 3rd, 4th, and 6th nerve palsy was 42, 15, and 11, respectively. Sixty patients experienced headache or orbital pain. 46 patients met the criteria for MVP. Among them, 31 patients had DO, and 15 non-diabetic patients also met the criteria for MVP. Of the 46 patients, 22 showed abnormalities on contrast-enhanced MRI. 19 patients were diagnosed with THS. In the diabetic and non-diabetic groups, 11 and 9 patients, respectively, were diagnosed with THS. The number of patients receiving steroid treatment in the diabetic and non-diabetic groups was 38 and 23, respectively, with pain relief rates within 3 days of 70 and 56%, p > 0.05.

Currently, the boundaries between DO, MVP, diabetes combined with THS, and benign THS remain unclear. There is a need for clinical research involving specialists in neurology, ophthalmology, and otolaryngology to establish standardized definitions, classifications, and diagnostic criteria.

## Linked entities

- **Diseases:** Tolosa-Hunt syndrome (MONDO:0018983)

## Full-text entities

- **Diseases:** pupil (MESH:D011681), trauma (MESH:D014947), sinusitis (MESH:D012852), muscle palsy (MESH:D019042), ischemia (MESH:D007511), eye pain (MESH:D058447), ischemic nerve infarction (MESH:D007238), type 2 diabetes (MESH:D003924), ocular motor nerve damage (MESH:D059348), sensory loss (MESH:C580162), neuropathy (MESH:D009422), vascular disease (MESH:D014652), atherosclerotic (MESH:D050197), hypoxia (MESH:D000860), DO (MESH:D003920), ischemic (MESH:D002545), viral meningitis (MESH:D008587), hypertension (MESH:D006973), ankylosing spondylitis (MESH:D013167), microvascular (MESH:D017566), mononeuritis ophthalmoplegia (MESH:D020422), Headache (MESH:D006261), benign ophthalmoplegia (MESH:D009886), herpes zoster virus infections (MESH:D006562), diplopia (MESH:D004172), Headache Disorders (MESH:D020773), coronary artery disease (MESH:D003324), tumors (MESH:D009369), ocular movement abnormalities (MESH:D015835), granulomatous inflammation (MESH:D007249), carotid artery siphon stenosis (MESH:D016893), infections (MESH:D007239), metabolic abnormalities (MESH:D008659), palsy (MESH:D010243), coronary atherosclerotic heart disease (MESH:D003327), cerebral infarction (MESH:D002544), diabetic oculomotor palsy (MESH:D015840), peripheral neuropathy (MESH:D010523), ocular muscle paralysis (MESH:D012133), brainstem infarction (MESH:D020526), Horner syndrome (MESH:D006732), stroke (MESH:D020521), myasthenia gravis (MESH:D009157), uremia (MESH:D014511), hyperglycemia (MESH:D006943), ischemic nerve damage (MESH:D000080902), pituitary adenomas (MESH:D010911), hyperlipidemia (MESH:D006949), cardiovascular and cerebrovascular diseases (MESH:D002318), cavernous sinus B-cell lymphoma (MESH:D016393), ocular muscle palsy (MESH:D009135), IOMP (MESH:D003389), orbital pain (MESH:D010146), ophthalmoplegic migraine (MESH:D060486), fourth cranial nerve palsy (MESH:D020432), ischemic demyelination (MESH:D003711), Fourth and sixth nerve palsy (MESH:D020434), impaired glucose tolerance (MESH:D018149), PO (MESH:C531833), alcohol abuse (MESH:D000437)
- **Chemicals:** glucose (MESH:D005947), steroid (MESH:D013256), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12310674/full.md

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Source: https://tomesphere.com/paper/PMC12310674