# Giant Cell Arteritis in the Third Decade of Life: A Case for Expanded Clinical Suspicion

**Authors:** Ogheneakpobor E Ubogun, Aishat T Alonge, Chinazo J Okenwa, Ifeoma L Ndigwe, Peace D Akhimienmhona

PMC · DOI: 10.7759/cureus.79262 · Cureus · 2025-02-18

## TL;DR

A 34-year-old woman with migraines was diagnosed with giant cell arteritis, a rare condition in young adults, highlighting the need for expanded clinical suspicion in similar cases.

## Contribution

This case report emphasizes the rarity of GCA in individuals under 50 and suggests a potential link between migraines and GCA.

## Key findings

- GCA was diagnosed in a 34-year-old woman with migraines through elevated inflammatory markers and ultrasound findings.
- Treatment with high-dose prednisolone led to remission of symptoms.
- The case highlights the importance of considering GCA in younger patients with migraines and atypical symptoms.

## Abstract

Giant cell arteritis (GCA), also known as temporal arteritis, is the most common idiopathic systemic vasculitis in middle-aged adults, predominantly involving large and medium-sized arteries. We report an unusual case of a 34-year-old woman with a five-year history of migraines who developed symptoms, including headache, transient vision loss, jaw claudication, and a 5 kg weight loss over two months. Physical examination revealed scalp tenderness, with no other notable findings. Laboratory investigations showed an elevated erythrocyte sedimentation rate (ESR) of 85 mm/hr and a C-reactive protein (CRP) level of 50 mg/L. Ultrasound of the temporal artery demonstrated thickening with the characteristic "halo" sign, and a biopsy confirmed inflammatory changes with multinucleated giant cells. Treatment with high-dose prednisolone resulted in remission, and the patient was discharged with a follow-up plan in place. GCA predominantly affects the superficial temporal arteries, with irreversible vision loss being its most serious complication. Prompt diagnosis and treatment are critical. The diagnosis relies on clinical features, elevated inflammatory markers, imaging studies, and histopathological confirmation. According to the European Alliance of Associations for Rheumatology (EULAR) guidelines, temporal artery ultrasound showing a non-compressible "halo" sign is recommended for diagnosis. Further studies are needed to investigate the potential connection between migraines and GCA. This case underscores the rarity of GCA in individuals under 50 and highlights the possibility of GCA developing in younger patients with a longstanding history of migraines.

## Linked entities

- **Diseases:** Giant cell arteritis (MONDO:0008538)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** GCA (MESH:D013700), weight loss (MESH:D015431), jaw claudication (MESH:D007383), headache (MESH:D006261), inflammatory (MESH:D007249), systemic vasculitis (MESH:D056647), migraines (MESH:D008881), vision loss (MESH:D014786), scalp tenderness (MESH:D063806)
- **Chemicals:** prednisolone (MESH:D011239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11926573/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11926573/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC11926573/full.md

---
Source: https://tomesphere.com/paper/PMC11926573