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Published on: February 8, 2019
Immunoglobulin G4-related aortitis mimicking an intramural hematoma
Daniel Z Tay1, Peter Y T Goh2, Terence K Teo2
1Mount Elizabeth Hospital (Orchard), Singapore daniel_jtzs@yahoo.com.sg.
Abstract:
Immunoglobulin G4-related systemic disease is a rare entity with various presenting symptoms. We report the case of a 34-year-old Chinese male who presented with immunoglobulin G4-related aortitis and the unusual symptom of hoarseness of voice. He underwent distal ascending aorta and total aortic arch replacement.
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