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Three young males with Hugh-Stovin’s syndrome presented with cough, haemoptysis, fever, raised inflammatory markers, and pulmonary artery aneurysm. Only one had recurrent oral ulcers suggestive of Behcet’s disease, and none were HLA B51 positive. All responded well to immunosuppression but eventually needed either an endovascular procedure or surgery.
Clinical Medicine Insights Arthritis and Musculoskeletal Disorders – SAGE
Published: May 1, 2023
Keywords: Hughes-Stovin syndrome; pulmonary artery aneurysm; Behcet’s disease; hepatic artery aneurysm; vascular embolization
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