Evaluation of clinical criteria for diagnosis of bullous pemphigoid

被引:143
作者
Vaillant, L [1 ]
Bernard, P
Joly, P
Prost, C
Labeille, B
Bedane, C
Arbeille, B
Thomine, E
Bertrand, P
Lok, C
Roujeau, JC
机构
[1] CHU Tours, Hop Trousseau, Dept Dermatol, F-37044 Tours, France
[2] Hop Dupuytren, Dept Dermatol, Limoges, France
[3] Hop Charles Nicolle, Dept Dermatol, Rouen, France
[4] Hop Charles Nicolle, Dept Pathol, Rouen, France
[5] Hop St Louis, Dept Dermatol, Paris, France
[6] Hop Henri Mondor, Dept Dermatol, F-94010 Creteil, France
[7] Hop Sud, Dept Dermatol, Amiens, France
[8] Hop Bretonneau, Dept Electron Microscopy, Tours, France
[9] Hop Bretonneau, Dept Electron Microscopy, Tours, France
[10] Hop Bretonneau, Dept Biostat, Tours, France
关键词
D O I
10.1001/archderm.134.9.1075
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Objective: To check the potential usefulness of clinical criteria for the diagnosis of bullous pemphigoid when state-of-the-art techniques such as Western immunoblotting, immunoprecipitation, and indirect immunofluorescence on salt-split skin or direct immunoelectron microscopy are not available. Design: Comparison of the clinical criteria between 2 groups (with and without bullous pemphigoid) as defined by immunoelectron microscopy used as standard criterion, in a prospective study. Multivariate logistic regression analysis was carried out by including all items that were statistically significant (at P < .05 level) in univariate analysis. Setting: Five dermatology departments in teaching hospitals. Patients: The 231 patients studied had subepidermal autoimmune bullous diseases with linear IgG or C3 deposits in the basement membrane zone (157 with bullous pemphigoid, 33 with cicatricial pemphigoid, 30 with epidermolysis bullosa acquisita, 5 with lupus erythematosus, and 6 others). A second set of patients was used to calculate predictive values. Results: The multivariate logistic stepwise analysis resulted in a final set of predictors that included only 4 items: absence of atrophic scars, absence of head and neck involvement, absence of mucosal involvement, and age greater than 70 years. No additional variables met the .05 significance level to enter into the model. If 3 of these 4 characteristics were present, a diagnosis of bullous pemphigoid could be made with a sensitivity of 90% and a specifity of 83%; these predictive values were calculated on a sample of 70 new cases. Conclusions: With an estimated incidence of bullous pemphigoid among subepidermal autoimmune bullous diseases of 80%, the presence of 3 of the 4 significant criteria allows the diagnosis of bullous pemphigoid, with a positive predictive value of 95%. Our set of clinical criteria thus allows the diagnosis of bullous bullous pemphigoid with good validity for both clinical practice and therapeutic trials.
引用
收藏
页码:1075 / 1080
页数:6
相关论文
共 44 条
[1]
CICATRICIAL PEMPHIGOID ANTIGEN DIFFERS FROM BULLOUS PEMPHIGOID ANTIGEN BY ITS EXCLUSIVE EXTRACELLULAR LOCALIZATION - A STUDY BY INDIRECT IMMUNOELECTRONMICROSCOPY [J].
BEDANE, C ;
PROST, C ;
BERNARD, P ;
CATANZANO, G ;
BONNETBLANC, JM ;
DUBERTRET, L .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (01) :3-9
[2]
BERNARD P, 1992, SPRINGER SEMIN IMMUN, V13, P401
[3]
INCIDENCE AND DISTRIBUTION OF SUBEPIDERMAL AUTOIMMUNE BULLOUS SKIN DISEASES IN 3 FRENCH REGIONS [J].
BERNARD, P ;
VAILLANT, L ;
LABEILLE, B ;
BEDANE, C ;
ARBEILLE, B ;
DENOEUX, JP ;
LORETTE, G ;
BONNETBLANC, JM ;
PROST, C .
ARCHIVES OF DERMATOLOGY, 1995, 131 (01) :48-52
[4]
THE MAJOR CICATRICIAL PEMPHIGOID ANTIGEN IS A 180-KD PROTEIN THAT SHOWS IMMUNOLOGICAL CROSS-REACTIVITIES WITH THE BULLOUS PEMPHIGOID ANTIGEN [J].
BERNARD, P ;
PROST, C ;
DUREPAIRE, N ;
BASSETSEGUIN, N ;
DIDIERJEAN, L ;
SAURAT, JH .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (02) :174-179
[5]
STUDIES OF CICATRICIAL PEMPHIGOID AUTOANTIBODIES USING DIRECT IMMUNOELECTRON MICROSCOPY AND IMMUNOBLOT ANALYSIS [J].
BERNARD, P ;
PROST, C ;
LECERF, V ;
INTRATOR, L ;
COMBEMALE, P ;
BEDANE, C ;
ROUJEAU, JC ;
REVUZ, J ;
BONNETBLANC, JM ;
DUBERTRET, L .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 94 (05) :630-635
[6]
HETEROGENEOUS BULLOUS PEMPHIGOID ANTIBODIES - DETECTION AND CHARACTERIZATION BY IMMUNOBLOTTING WHEN ABSENT BY INDIRECT IMMUNOFLUORESCENCE [J].
BERNARD, P ;
DIDIERJEAN, L ;
DENIS, F ;
SAURAT, JH ;
BONNETBLANC, JM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 92 (02) :171-174
[7]
BHOGAL BS, 1990, MANAGEMENT BLISTERIN, P15
[8]
CICATRICIAL PEMPHIGOID - IDENTIFICATION OF 2 DISTINCT SETS OF EPIDERMAL ANTIGENS BY IGA AND IGG CLASS CIRCULATING AUTOANTIBODIES [J].
CHAN, LS ;
HAMMERBERG, C ;
COOPER, KD .
ARCHIVES OF DERMATOLOGY, 1990, 126 (11) :1466-1468
[9]
CHORZELSKI TP, 1979, BRIT J DERMATOL, V101, P535, DOI 10.1111/j.1365-2133.1979.tb11882.x
[10]
ISOLATION OF A HUMAN EPIDERMAL CDNA CORRESPONDING TO THE 180-KD AUTOANTIGEN RECOGNIZED BY BULLOUS PEMPHIGOID AND HERPES-GESTATIONIS SERA - IMMUNOLOCALIZATION OF THIS PROTEIN TO THE HEMIDESMOSOME [J].
DIAZ, LA ;
RATRIE, H ;
SAUNDERS, WS ;
FUTAMURA, S ;
SQUIQUERA, HL ;
ANHALT, GJ ;
GIUDICE, GJ .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) :1088-1094