Related Experiment Video
Updated: Jun 28, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Wegener's granulomatosis
Lawrence W Weeda1, Stephen A Coffey
1Department of Oral and Maxillofacial Surgery, University of Tennessee, College of Dentistry, 875 Union Avenue, Memphis, TN 38163, USA. lweeda@utmem.edu
Abstract:
WG is an uncommon disease process with considerable risk of mortality if diagnosis and treatment are delayed. Skin, sinus, or oral mucosal lesions may be part of the initial presentation. This article provided the clinician with information concerning recognition, diagnosis, and treatment of WG. Early recognition and treatment are essential in limiting the potentially life-threatening aspects of the disease.
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