Myoepithelioma is a rare tumor accounting for less than 1. 5 % of all salivary gland tumors , Clinically , myeopithelioma present as slow − growing , painless masses and cannot be distinguished from pleomorphic adenoma . We report a case of myoepithelioma of the palate . The patient was a 5レ year − 01d woman who had a painless mass on the palate . On magnetic resonance image, the 皿 ass showed slightiy high signal intensity on T1 − weighted images enhanced
The case was a 39 − year − Qld male , and the chief complaint was swelling in the bottom jawbone of the left side , and it consulted the our department on March 工 ,2003 . Although it was diagnosed as odontogenic infection , diabetes was controlled , while performing reduction − of − inflammation treatments , such as medication of the antibiotic after hospita正 iza − tion, and incision , since it was l type diabetes in a poor control state . Although progress was good , it shifted to a shock state and DIC from enteritis condition after that. The supple − ment treatment by the toxin absorption treatment , the anti − solidification treatment , blood platelet transfusion, antibiotic medication , etc , were performed , and condition has improved in about two weeks . It was thought that the cause concurred with MRSA enteritis from the bacillus shift phenomenon by use of the antibiotic used into the reduction − of − i1 ユflammation treatment . The difficulty of the diagnosis of a diabetic ' s tooth sexually transmitted disease and disposal was reconfirmed .
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