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Review Question - QID 213647

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QID 213647 (Type "213647" in App Search)
A 75-year-old woman presents to the physician with complaint of a new headache on her right side that she describes as “throbbing” and continuous. She notes that she experiences focal tenderness when she directly pushes on the right side of her head and also with combing her hair. When questioned about other symptoms, she notes that she has felt fatigue and discomfort in her jaw muscles when chewing her food. In addition, she has been concerned about 1 episode of painless vision loss in her right eye that lasted for about 1 minute before her normal vision was restored. An arterial biopsy is performed and confirms the diagnosis. Which of the following findings was most likely seen on pathology?

Focal granulomatous inflammation

81%

150/185

Granulomatous, necrotizing inflammation with eosinophilia

5%

9/185

IgA immune complex deposition

0%

0/185

Non-granulomatous, necrotizing inflammation

4%

8/185

“Onion-skin” appearance of the arteriolar wall

3%

5/185

Select Answer to see Preferred Response

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This elderly female patient with unilateral headache, jaw claudication, and painless transient vision loss most likely has temporal giant cell arteritis, which features focal granulomatous inflammation on pathology.

Temporal giant cell arteritis is a large-vessel vasculitis that is typically seen in female patients over 50 years of age and presents with headache in the temporal region, jaw claudication, and occasionally visual symptoms, such as amaurosis fugax (transient vision loss). Giant cell arteritis should always be considered in the differential diagnosis of a patient with new-onset headache in elderly patients with an elevated erythrocyte sedimentation rate (ESR). Diagnosis is confirmed with a temporal artery biopsy, which shows hallmark histological features of vessel thickening with a narrowed lumen, granulomatous inflammation, and presence of giant cells (Illustration A). Permanent vision loss may occur in up to 20% of patients if prompt initiation of treatment with corticosteroids is not performed.

Illustration A shows a temporal artery biopsy specimen from a patient with giant cell arteritis, with the arrow pointing to a giant cell.

Incorrect Answers:
Answer 2: Granulomatous, necrotizing inflammation of the arterial wall with eosinophilia is characteristic of eosinophilic granulomatosis with polyangiitis, a small-vessel vasculitis that presents with asthma, sinusitis, skin nodules or purpura, and peripheral neuropathy.

Answer 3: IgA immune complex deposition in the arterial wall is characteristic of IgA vasculitis, which is most commonly seen in children and presents with a triad of skin findings (palpable purpura), arthralgias, and abdominal pain.

Answer 4: Non-granulomatous, necrotizing inflammation of the arterial wall is characteristic of microscopic polyangiitis, a vasculitis which commonly involves the lung, kidneys, and skin.

Answer 5: “Onion-skin” appearance of the arterial wall is characteristic of hyperplastic arteriosclerosis, a condition most commonly associated with hypertensive emergency.

Bullet Summary:
Focal granulomatous inflammation with giant cells is seen on pathology in giant cell arteritis.

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