Brunsting-Perry pemphigoid: a systematic review.
Italo Francesco AromoloCarlo Alberto MaroneseChiara MoltrasioGiovanni GenoveseAngelo Valerio MarzanoPublished in: International journal of dermatology (2022)
BPP nosologic position remains uncertain, given the overlap with other autoimmune bullous diseases, such as MMP, bullous pemphigoid, and epidermolysis bullosa acquisita, particularly in its BPP-like variant. Nonpredominant oral mucosal lesions may appear during the course of the disease, generally after cutaneous manifestations. Positivity of DIF and anti-BP180/230 autoantibodies detected on ELISA/immunoblotting in the absence of anticollagen VII antibodies may provide guidance in diagnosing BPP.