作者: O. MORI , H. HACHISUKA , M. KUSUHARA , Y. SASAI , S. FUJIWARA
DOI: 10.1111/J.1365-2133.1994.TB02909.X
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摘要: Summary We report a 19-year-old woman with typical clinical histological and immunofluorescence features of bullous pemphigoid. By immunoblotting, the serum was shown to detect antigens at 240 138 kDa. Elevated IgK levels were present, there marked peripheral blood eosinophilia. The degree eosinophilia correlated small changes in severity skin lesions, IgE level showed correlation severity. Another unusual feature an exacerbation her disease time first menses after onset