Amicrobial pustular dermatosis of cutaneous folds associated with autoimmune disorders: A new entity?

被引:37
作者
Marzano, AV
Capsoni, F
Berti, E
Gasparini, G
Bottelli, S
Caputo, R
机构
[1] Institute of Dermatological Sciences, University of Milan, IRCCS, Milan, Ospedale Maggiore
[2] Institute of Internal Medicine, University of Milan, IRCCS, Milan, Ospedale Maggiore
关键词
autoimmune diseases; lupus erythematosus; neutrophilic dermatoses; neutrophils; subcorneal pustular dermatosis;
D O I
10.1159/000246219
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: An unclassified amicrobial pustular dermatosis particularly affecting the main cutaneous folds, external auditory canals and scalp and coexisting with systemic lupus erythematosus has been recently described. Objective: We studied 3 young females bearing such cutaneous manifestations in association with subacute cutaneous lupus erythematosus, celiac disease and various serum autoantibodies, respectively, in order to further characterize this possibly new entity. Methods: Various routine and immunological laboratory tests, histopathologic and direct immunofluorescence examinations and in vitro studies of neutrophil function were performed in each patient. Results: We reported our findings and compared our cases with the few others appearing in the literature. We documented an impaired neutrophil chemotaxis in 2 subjects, but neutrophil dysfunction does not seem to be one of the verifying criteria. Conclusions: All of these cases may represent a distinctive form in the clinicopathological spectrum of neutrophilic dermatoses (ND) because of the typical distribution and the close link with different autoimmune disorders. Cimetidine in combination with ascorbic acid can be indicated as an effective and safe alternative to the classic medications of ND, although the action of both drugs remains unexplained.
引用
收藏
页码:88 / 93
页数:6
相关论文
共 23 条
[1]  
BUFFET C, 1987, GASTROEN CLIN BIOL, V11, P828
[2]   INVITRO AND EXVIVO EFFECT OF RU41740 ON HUMAN POLYMORPHONUCLEAR LEUKOCYTE FUNCTION [J].
CAPSONI, F ;
MINONZIO, F ;
VENEGONI, E ;
ONGARI, AM ;
MERONI, PL ;
GUIDI, G ;
ZANUSSI, C .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1988, 10 (02) :121-133
[3]  
CRICKX B, 1991, JOURN DERM PAR 6 9 M
[4]  
DELAPORTE E, 1992, ACTA DERM-VENEREOL, V72, P301
[5]   HYPERIMMUNOGLOBULIN-E SYNDROME - RESPONSE TO TRANSFER-FACTOR AND ASCORBIC-ACID THERAPY [J].
FRIEDENBERG, WR ;
MARX, JJ ;
HANSEN, RL ;
HASELBY, RC .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1979, 12 (02) :132-142
[6]  
LABEILLE B, 1987, ANN DERMATOL VENER, V114, P1411
[7]   PHAGOCYTE FUNCTION AND CELL-MEDIATED-IMMUNITY IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
LANDRY, M .
ARCHIVES OF DERMATOLOGY, 1977, 113 (02) :147-154
[8]  
Lehrer R., 1981, METHODS STUDYING MON, P693
[9]   HEMALOG-D WHITE CELL DIFFERENTIAL SYSTEM [J].
MANSBERG, HP ;
SAUNDERS, AM ;
GRONER, W .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1974, 22 (07) :711-724
[10]   THE HYPERIMMUNOGLOBULIN-E SYNDROME - A NEUTROPHIL CHEMOTACTIC DEFECT REVERSIBLE BY HISTAMINE H-2-RECEPTOR BLOCKADE [J].
MAWHINNEY, H ;
KILLEN, M ;
FLEMING, WA ;
ROY, AD .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1980, 17 (04) :483-491