JAPANESE JOURNAL OF ORAL & MAXILLOFACIAL SURGERY | |
Vol. 55 No. 3 2009 | |
ISSN: 0021-5163 UBIC: 151-J | |
ABSTRACT | |
Hereditary angioedema (HAE) is a rare disease caused by functional disorder or a reduction in C1 inhibitor (C1-INH). HAE was first described
by Osler in 1888. Dental treatment and oral surgery in HAE patients can trigger life-threatening laryngeal edema. C1-INH is effective for both the prevention of HAE
and the treatment of acute attacks. Since C1-INH is a blood product and very expensive in Japan, C1-INH should be used carefully. Other drugs or methods should also
be considered to prevent attacks of HAE. We report a male patient with HAE who required tooth extraction. To prevent angioedema associated with tooth extraction, the
patient was given tranexamic acid before operation. He underwent tooth extraction after receiving intravenous propofol and midazolam. He was observed during the night
after the operation and was discharged from the hospital the next morning, without any complications.
Keywords: hereditary angioedema, tooth extraction, C1 inhibitor. |
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