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Published on: June 23, 2014
A Rare Presentation of Polyarteritis Nodosa
Ciji Robinson1, Zarqa Yasin1, Parth Patel1
1Internal Medicine, Henry Ford Health System, Jackson, USA.
Polyarteritis nodosa (PAN), a rare vasculitis, can affect multiple organs. This case highlights mesenteric artery involvement diagnosed via CTA and treated successfully with steroids, even without biopsy confirmation.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Immunology
Background:
- Polyarteritis nodosa (PAN) is a rare, necrotizing medium-vessel vasculitis with potential for systemic organ damage.
- Commonly affects skin, renal, neurologic, and musculoskeletal systems, with diagnosis often confirmed by biopsy.
- Mesenteric artery involvement in PAN, while less common, presents diagnostic and therapeutic challenges.
Observation:
- A 66-year-old female presented with chest and epigastric pain.
- Computed tomography angiography revealed characteristic PAN findings in the mesenteric arteries: alternating narrowing and aneurysmal dilation.
- Biopsy of the affected mesenteric arteries was deemed too risky and not performed.
Findings:
- Elevated erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) supported systemic inflammation.
- Extensive infectious disease workup yielded negative results, ruling out infectious causes.
- Clinical improvement and full recovery following high-dose steroid therapy strongly indicated PAN.
Implications:
- This case underscores the utility of computed tomography angiography in diagnosing PAN, particularly when biopsy is contraindicated.
- It highlights the effectiveness of high-dose steroids as a primary treatment for PAN, even in complex cases with mesenteric involvement.
- The successful management emphasizes the importance of considering PAN in patients with unexplained abdominal pain and inflammatory markers, even without typical organ involvement.
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