Bullous pemphigoid and dermatitis herpetiformis association: A genetic predisposition

2013 ◽  
Vol 40 (11) ◽  
pp. 940-941 ◽  
Author(s):  
Fabrizio Vaira ◽  
Valentina Della Valle ◽  
Daniele Fanoni ◽  
Paolo Pontini ◽  
Simona Muratori
Keyword(s):  
Bullous Pemphigoid ◽  
Genetic Predisposition ◽  
Dermatitis Herpetiformis

Genetic predisposition to bullous pemphigoid

2020 ◽  
Vol 100 (2) ◽  
pp. 86-91
Author(s):  
Jieyu Zhang ◽  
Gang Wang
Keyword(s):  
Bullous Pemphigoid ◽  
Genetic Predisposition

scholarly journals Bullous Systemic Lupus Erythematosus

2018 ◽  
Vol 19 (2) ◽  
pp. 123-125
Author(s):  
Sk Jakaria Been Sayeed ◽  
Md Mujibur Rahman ◽  
AKM Humayon Kabir ◽  
Md Moniruzzaman ◽  
Uzzal Mallik ◽  
...  
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Bullous Pemphigoid ◽  
Epidermolysis Bullosa ◽  
Lupus Erythematosus ◽  
Dermatitis Herpetiformis ◽  
Epidermolysis Bullosa Acquisita ◽  
Systemic Lupus ◽  
Type Vii Collagen ◽  
Linear Iga Disease ◽  
Distinct Disease

Bullous systemic lupus erythematosus (BSLE) is extremely rare but distinct disease, characterized by vesicobullous skin eruptions in systemic lupus erythematosus (SLE). It can develop either before or after a diagnosis of SLE has been established. BSLE is characterized by a dermatitis herpetiformis-like histology and an autoimmunity to type VII collagen. It must be differentiated from other autoimmune vesicobullous diseases such as epidermolysis bullosa acquisita, dermatitis herpetiformis, linear IgA disease, and bullous pemphigoid. Its important to combine clinical, histological, and immunofluorescence findings to establish a diagnosis of BSLE. We report a case of BSLE to illustrate and emphasize the need for an integrative diagnostic approach.J MEDICINE JUL 2018; 19 (2) : 123-125

Histology of linear IgA disease, dermatitis herpetiformis, and bullous pemphigoid

1983 ◽  
Vol 5 (6) ◽  
pp. 547-554 ◽  
Author(s):  
W. K. Blenkinsopp ◽  
G. P. Haffenden ◽  
L. Fry ◽  
J. N. Leonard
Keyword(s):  
Bullous Pemphigoid ◽  
Dermatitis Herpetiformis ◽  
Linear Iga Disease

Expression of selected ADAMs in bullous pemphigoid and dermatitis herpetiformis

2009 ◽  
Vol 56 (1) ◽  
pp. 58-61 ◽  
Author(s):  
Agnieszka Zebrowska ◽  
Malgorzata Wagrowska-Danilewicz ◽  
Marian Danilewicz ◽  
Karolina Wodz ◽  
Milena Sokolowska ◽  
...  
Keyword(s):  
Bullous Pemphigoid ◽  
Dermatitis Herpetiformis

scholarly journals The Role of Intereukin-31 in Pathogenesis of Itch and Its Intensity in a Course of Bullous Pemphigoid and Dermatitis Herpetiformis

2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Lilianna Kulczycka-Siennicka ◽  
Anna Cynkier ◽  
Elżbieta Waszczykowska ◽  
Anna Woźniacka ◽  
Agnieszka Żebrowska
Keyword(s):  
Signaling Pathway ◽  
Bullous Pemphigoid ◽  
Dermatitis Herpetiformis ◽  
Subjective Symptoms ◽  
Autoimmune Blistering Disease ◽  
Stat Signaling ◽  
Blistering Disease ◽  
Autoimmune Blistering Diseases

Itch which is one of the major, subjective symptoms in a course of bullous pemphigoid and dermatitis herpetiformis makes those two diseases totally different than other autoimmune blistering diseases. Its pathogenesis is still not fully known. The aim of this research was to assess the role of IL-31 in development of itch as well as to measure its intensity. Obtained results, as well as literature data, show that lower concentration of IL-31 in patients’ serum may be correlated with its role in JAK/STAT signaling pathway which is involved in development of autoimmune blistering disease. Intensity of itch is surprisingly huge problem for the patients and the obtained results are comparable with results presented by atopic patients.

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