Immunoglobulin G4-related aortitis mimicking an intramural hematoma

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 ar...

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Veröffentlicht in:Asian cardiovascular & thoracic annals 2015-11, Vol.23 (9), p.1083-1086
Hauptverfasser: Tay, Daniel Z, Goh, Peter YT, Teo, Terence K, Boey, Mee Leng, Chachlani, Naresh, Wong, Poo Sing
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Sprache:eng
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Zusammenfassung: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.
ISSN:0218-4923
1816-5370
DOI:10.1177/0218492314533974