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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Published in: | Asian cardiovascular & thoracic annals Vol. 23; no. 9; pp. 1083 - 1086 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
London, England
SAGE Publications
01-11-2015
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Subjects: | |
Online Access: | Get full text |
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Summary: | 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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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0218-4923 1816-5370 |
DOI: | 10.1177/0218492314533974 |