A TYPICAL CASE OF PEMPHIGOID GESTATIONIS WITH A UNIQUE PATTERN OF INTERCELLULAR IMMUNOFLUORESCENCE

Citation
Sav. Jones et al., A TYPICAL CASE OF PEMPHIGOID GESTATIONIS WITH A UNIQUE PATTERN OF INTERCELLULAR IMMUNOFLUORESCENCE, British journal of dermatology, 136(2), 1997, pp. 245-248
Citations number
11
Categorie Soggetti
Dermatology & Venereal Diseases
ISSN journal
00070963
Volume
136
Issue
2
Year of publication
1997
Pages
245 - 248
Database
ISI
SICI code
0007-0963(1997)136:2<245:ATCOPG>2.0.ZU;2-E
Abstract
Pemphigoid gestationis is an autoimmune bullous disorder affecting pre gnant women which typically presents in the second and third trimester of pregnancy with an itchy bullous eruption on the abdomen and limbs. The diagnosis is confirmed by the presence of complement-binding IgG antibasement membrane zone (BMZ) antibodies, which bind to the roof of salt-split skin. We describe a case of clinically typical pemphigoid gestationis with the combination of intercellular IgG and BMZ IgG and C3 staining on immunofluorescence, a pattern which is unique for this condition.