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Diagnosis of Giant Cell Arteritis

Blood test sample labelled Anti C1q Antibody held by gloved hand

Anti C1q antibody tests can support the diagnosis of inflammatory diseases like Giant Cell Arteritis.

Diagnosis of Giant Cell Arteritis

The diagnosis of giant cell arteritis requires a combination of clinical evaluation, blood tests, imaging, and—when needed—biopsy. Because giant cell arteritis can cause irreversible complications such as vision loss or stroke, early and accurate diagnosis is vital. Treatment is often initiated based on strong clinical suspicion even before confirmation, due to the high risk of delay.

This condition most commonly affects people over the age of 50, and the diagnostic process often begins when a patient presents with symptoms such as new-onset headache, jaw pain, or visual disturbances.

Clinical Evaluation

A detailed history and physical examination are the first steps. Key features that suggest GCA include:

New, persistent headaches in people over 50

Jaw claudication

Tenderness or thickening of the temporal arteries

Scalp sensitivity

Visual symptoms, such as blurred or double vision

Symptoms of polymyalgia rheumatica

On examination, doctors may find:

Thick, tender, or pulseless temporal arteries

Asymmetry in arterial pulses

Bruits (abnormal whooshing sounds) over large vessels

Signs of ischaemia, such as pale retina or afferent pupillary defect

Blood Tests

Although not diagnostic on their own, blood tests provide crucial supporting evidence.

1. Erythrocyte Sedimentation Rate (ESR)

Often markedly elevated (typically over 50 mm/hr)

Reflects systemic inflammation

2. C-Reactive Protein (CRP)

Sensitive marker for inflammation

May be raised even if ESR is normal

3. Full Blood Count

May show normochromic, normocytic anaemia

Thrombocytosis (elevated platelet count) is also common

These results support a clinical diagnosis and help rule out other causes.

Temporal Artery Biopsy

The gold standard for diagnosis is a temporal artery biopsy, which involves removing a small section of artery from the temple for microscopic examination.

Key findings include:

Granulomatous inflammation

Multinucleated giant cells

Intimal thickening and vessel wall disruption

While this is a highly specific test, false negatives can occur due to “skip lesions”, where inflammation affects segments of the artery unevenly. To reduce this risk, longer biopsy samples (2–3 cm) are preferred.

Biopsy should be performed within 1–2 weeks of starting steroids, as treatment can begin to reduce inflammatory changes quickly.

Imaging Studies

Modern imaging techniques have become valuable in both diagnosing and monitoring giant cell arteritis, especially in cases where biopsy is not possible.

1. Ultrasound (Colour Doppler)

Can detect the “halo sign”—a dark, hypoechoic ring around the artery indicating inflammation

Non-invasive, fast, and increasingly used as a first-line test

2. MRI or CT Angiography

Used to visualise larger arteries, such as the aorta or subclavian arteries

Helps assess extent of vessel involvement and detect complications like aneurysms

3. FDG-PET Scan

Useful in systemic or atypical cases

Detects increased metabolic activity in inflamed arteries

Expensive and less widely available

Diagnostic Criteria

The American College of Rheumatology (ACR) criteria for diagnosis include:

Age over 50

New-onset localised headache

Tenderness or decreased pulse in temporal artery

ESR > 50 mm/hr

Abnormal biopsy

Meeting three or more of these criteria yields high diagnostic accuracy, though real-world diagnosis often relies on a combination of clinical judgement and test results.

Differential Diagnosis

Conditions that can mimic GCA include:

Tension or migraine headaches

Dental infections

Trigeminal neuralgia

Carotid artery dissection

Meningitis or subarachnoid haemorrhage

These possibilities must be ruled out, especially when symptoms are non-specific or when typical GCA features are absent.

Initiating Treatment Before Confirmation

Due to the risk of permanent vision loss, treatment with high-dose corticosteroids should begin immediately if GCA is strongly suspected—even before biopsy or imaging confirmation.

Diagnosis of Giant Cell Arteritis

Delaying treatment can result in devastating consequences, and early steroid use does not invalidate a biopsy for at least 7–10 days.

[Next: Treatment of Giant Cell Arteritis→]

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