# Extensive Cerebral Venous Sinus Thrombosis in a Young Male With Severe Hyperhomocysteinaemia: An Unusual Presentation With Early Diplopia

**Authors:** Sooraj Narayan, Balaji Kombde, Atish Komwad

PMC · DOI: 10.7759/cureus.102233 · Cureus · 2026-01-24

## TL;DR

A young man with a rare brain vein blood clot had high homocysteine levels and developed double vision during treatment.

## Contribution

Highlights hyperhomocysteinaemia as a critical but overlooked risk factor in young patients with cerebral venous sinus thrombosis.

## Key findings

- A 25-year-old male with no prior health issues developed CVST with elevated homocysteine levels.
- Early diplopia occurred due to abducens nerve palsy during treatment, managed with acetazolamide and prisms.
- The case underscores the need to evaluate metabolic factors in young CVST patients.

## Abstract

Cerebral venous sinus thrombosis (CVST) is a rare cause of stroke, particularly in young adults, and often presents with nonspecific symptoms that may delay diagnosis. Hyperhomocysteinaemia is a recognized but frequently overlooked prothrombotic risk factor. We report a case of a 25-year-old previously healthy male who presented with sudden-onset severe unilateral headache and projectile vomiting. Neuroimaging with magnetic resonance imaging and venography revealed extensive thrombosis involving the superior sagittal, left transverse, and left sigmoid sinuses with cortical veins involvement. Laboratory evaluation showed markedly elevated serum homocysteine levels, with no other identifiable risk factors.

The patient was treated with therapeutic anticoagulation, osmotic agents, and vitamin supplementation for hyperhomocysteinaemia. During treatment, he developed early horizontal diplopia due to left abducens nerve palsy, attributed to evolving intracranial hypertension. Acetazolamide with Fresnel prism eye glasses led to stabilization and gradual improvement of symptoms. This case emphasizes the importance of evaluating metabolic risk factors such as hyperhomocysteinaemia in young patients with CVST and highlights the need for vigilant clinical monitoring for neurological deterioration even after initiation of appropriate therapy.

## Linked entities

- **Chemicals:** homocysteine (PubChem CID 778), acetazolamide (PubChem CID 1986)
- **Diseases:** abducens nerve palsy (MONDO:0007033), intracranial hypertension (MONDO:0006810)

## Full-text entities

- **Genes:** F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, MTHFR (methylenetetrahydrofolate reductase) [NCBI Gene 4524], PROC (protein C, inactivator of coagulation factors Va and VIIIa) [NCBI Gene 5624] {aka APC, PC, PROC1, THPH3, THPH4}, THBD (thrombomodulin) [NCBI Gene 7056] {aka AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM}
- **Diseases:** arterial stroke (MESH:D020243), neurological deterioration (MESH:D009422), esotropia (MESH:D004948), nasal blockage (MESH:D015508), limitation of abduction (MESH:D045745), LS (MESH:D007888), Hyperhomocysteinemia (MESH:D020138), intracranial hypertension (MESH:D019586), hemorrhagic infarction (MESH:D007238), dehydration (MESH:D003681), venous thrombosis (MESH:D020246), antiphospholipid syndrome (MESH:D016736), cerebrovascular disorder (MESH:D002561), infections (MESH:D007239), Diplopia (MESH:D004172), subarachnoid hemorrhage (MESH:D013345), carpopedal spasm (MESH:D013035), thrombosis (MESH:D013927), pressure (MESH:D003668), maxillary sinusitis (MESH:D015523), vomiting (MESH:D014839), APS (MESH:D016884), metabolic abnormalities (MESH:D008659), seizures (MESH:D012640), neurological deficits (MESH:D009461), pulmonary embolism (MESH:D011655), abducens nerve palsy (MESH:D020434), motor, sensory, or cerebellar deficits (MESH:D002526), fever (MESH:D005334), vitamin B12 deficiency (MESH:D014806), venous congestion (MESH:D006940), stroke (MESH:D020521), cerebral venous thrombosis (MESH:D020767), cerebral edema (MESH:D001929), intracranial hemorrhage (MESH:D020300), hemorrhage (MESH:D006470), intracranial space-occupying lesions (MESH:D020765), edema (MESH:D004487), venous involvement (MESH:D014689), CVST (MESH:D012851), venous infarction (MESH:D020520), endothelial dysfunction (MESH:D014652), visual disturbances (MESH:D014786), pain (MESH:D010146), head trauma (MESH:D006259), multi-sinus involvement (MESH:D012852), headache (MESH:D006261), papilledema (MESH:D010211)
- **Chemicals:** folate (MESH:D005492), calcium (MESH:D002118), vitamin B6 (MESH:D025101), heparin (MESH:D006493), alcohol (MESH:D000438), vitamin B12 (MESH:D014805), mannitol (MESH:D008353), Homocysteine (MESH:D006710), sulfur-containing amino acid (-), nitric oxide (MESH:D009569), calcium gluconate (MESH:D002125), Acetazolamide (MESH:D000086), methionine (MESH:D008715)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C677T

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12930108/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930108/full.md

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Source: https://tomesphere.com/paper/PMC12930108