scholarly journals Idiopathic bullous eosinophilic cellulitis (Wells syndrome) responsive to topical tacrolimus and antihistamine combination

2012 ◽  
Vol 78 (3) ◽  
pp. 378 ◽  
Author(s):  
Prashant Verma ◽  
Sonal Sharma ◽  
Archana Singal
2018 ◽  
Vol 149 (suppl_1) ◽  
pp. S59-S59
Author(s):  
Jehan Abdulsattar ◽  
Yasir AlZubaidi ◽  
Nestor Dela Cruz

2018 ◽  
Vol 4 (6) ◽  
pp. 548-550 ◽  
Author(s):  
Sandra Herout ◽  
Wolfgang Michael Bauer ◽  
Christopher Schuster ◽  
Georg Stingl

Reumatismo ◽  
2020 ◽  
Vol 71 (4) ◽  
pp. 226-229
Author(s):  
N. Belfeki ◽  
E. Gharbi ◽  
C. Flateau ◽  
S. Diamantis

Wells’ syndrome, also called eosinophilic cellulitis, is a rare eosinophilic dermatosis characterized by an unspecific inflammatory erythematous eruption often associated with systemic symptoms. Here we report the case of a 57-year-old female with bilateral painful pitting and pruritic feet progressive for two weeks despite one week of oral antibiotics. Skin biopsy was performed showing dermal eosinophilic infiltration. The patient showed a spontaneous progressive improvement of the condition. The presented case demonstrates both clinical and histologic presence of lesions of Wells’ syndrome in the course of the disease. A careful diagnostic approach is needed because of the lack of specific signs. The global outcome is favorable and spontaneous resolution is possible.


2017 ◽  
Vol 16 (1) ◽  
pp. 24
Author(s):  
Yu. G. Haliulin ◽  
K. A. Pavlov ◽  
M. P. Chan ◽  
E. M. Dzybova ◽  
E. A. Vasilevskaya

Dermatology ◽  
1988 ◽  
Vol 176 (6) ◽  
pp. 299-304 ◽  
Author(s):  
M.C. Ferrier ◽  
A. Janin-Mercier ◽  
P. Souteyrand ◽  
M. Bourges ◽  
C. Hermier

2020 ◽  
Vol 100 (18) ◽  
pp. adv00332
Author(s):  
M Blomberg ◽  
C Winther ◽  
S Høyrup ◽  
L Skov

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