Results 151 to 160 of about 23,997 (201)

Epidermolysis Bullosa Acquisita: A Case Report of a Rare Clinical Phenotype and a Review of Literature. [PDF]

Cureus, 2019
Beiu C, Mihai M, Popa L, Tebeica T, Giurcaneanu C.   +4 more
europepmc   +1 more source

International Bullous Diseases Group: consensus on diagnostic criteria for epidermolysis bullosa acquisita

British Journal of Dermatology, 2018
C. Prost-Squarcioni, F. Caux, Enno Schmidt, M. Jonkman, S. Vassileva, Soo-Chan Kim, P. Iranzo, M. Daneshpazhooh, Jorrit B. Terra, Johann W. Bauer, J. Fairley, Russell P. Hall, M. Hertl, Julia S. Lehman, B. Marinović, A. Patsatsi, D. Zillikens, V. Werth, D. Woodley, D. Murrell   +19 more
semanticscholar   +1 more source

Erytrodermic epidermolysis bullosa acquisita [PDF]

, 2014
Borradori, Luca, Häfliger, Stefanie, Klötgen, Hans-Willhelm   +2 more
core  

Accessible Diagnostic Methods to Differentiate between Epidermolysis Bullosa Acquisita and Other Subepidermal Autoimmune Bullous Diseases. [PDF]

Indian J Dermatol, 2018
Kridin K.
europepmc   +1 more source

Delayed-Onset Localized Bullous Pemphigoid on an Umbilical Hernia Repair Scar: An Example of Ruocco's Immunocompromised Cutaneous District. [PDF]

Cureus
Tercan E, Cetinarslan T, Temiz P, Sagcan Tercan SY, Ermertcan AT.   +4 more
europepmc   +1 more source

Epidermolysis Bullosa Acquisita

The American Journal of Dermatopathology, 1988
A case of epidermolysis bullosa acquisita (EBA) occurring in a 30 year-old-farmer is described. Diagnosis was suggested by clinical signs (adult-onset of mechano-bullous lesions healing with atrophic scar and milia formation, in absence of family history, photosensitivity and urine darkening); it was confirmed by laboratory data (normal urinary ...
PISANI M, RUOCCO, Vincenzo, DE ANGELIS E.   +2 more
core   +5 more sources

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Management of Epidermolysis Bullosa Acquisita

Dermatologic Clinics, 2011
Epidermolysis bullosa acquisita is a rare and debilitating autoimmune mucocutaneous blistering disease caused by autoantibodies directed against type VII collagen or anchoring fibrils in the subepidermal basement membrane zone. Treatment is quite challenging because this disease can be recalcitrant to multiple modalities.

exaly   +3 more sources

Epidermolysis Bullosa Acquisita Localized to the Face

Journal of Dermatology, 1998
A 39-year-old woman had a three-year history of recurrent bullous eruption localized to her left cheek. The diagnosis of epidermolysis bullosa acquisita was confirmed by means of direct immunofluorescence and direct immunoelectron microscopic studies ...
Soo-Chan Kim, Eun-So Lee, G S Choi
exaly   +2 more sources

Treatment of Recurrent Epidermolysis Bullosa Acquisita With Tofacitinib.

JAMA dermatology, 2023
This case report describes a patient with recurrent epidermolysis bullosa acquisita who was treated with tofacitinib.
Birao Fan, Ming-Yue Wang
semanticscholar   +1 more source