Results 61 to 70 of about 24,870 (249)
Striking enhancement at the site of radiation for nivolumab-induced Stevens-Johnson syndrome [PDF]
, 2018 Stevens-Johnson syndrome is a rare adverse cutaneous drug reaction characterized by epidermal detachment of
Al-Omari, Ahmed +2 more
core
Immunoglobulin E-Mediated Autoimmunity [PDF]
, 2018 The study of autoimmunity mediated by immunoglobulin E (IgE) autoantibodies, which may be termed autoallergy, is in its infancy. It is now recognized that systemic lupus erythematosus, bullous pemphigoid (BP), and chronic urticaria, both spontaneous and ...
Altrichter, Sabine +5 more
core +1 more source
A case report of bullous pemphigoid following secukinumab therapy for a patient with psoriasis
Journal of Dermatological TreatmentAim: Bullous pemphigoid induced by secukinumab in treatment of psoriasis is rare.Methods: We report a 49-year-old man with psoriasis who developed bullous pemphigoid during treatment with secukinumab.Results: Scattered tense vesicles with itching ...
Guanghan Wang +3 more
doaj +1 more source
Acta Dermato-Venereologica, 2018 Oesophageal involvement in mucous membrane pemphigoid is considered rare, but it may be underdiagnosed. To assess the incidence of oesophageal involvement in a group of patients with newly diagnosed mucous membrane pemphigoid we retrospectively analysed ...
Sandrine Benoit +3 more
doaj +1 more source
Frontiers in Immunology, 2020 Objectives: The clinical outcome of bullous pemphigoid appears worse in patients with infectious complications, and assessment of the prevalence and risk factors of infectious complications could be necessary to plan preventative strategies and to ...
Jia Chen +9 more
doaj +1 more source
JEADV Clinical Practice, EarlyView.ABSTRACT Background In ocular mucous membrane pemphigoid (MMP) direct immunofluorescence (DIF) represents the gold standard for definitive diagnosis. However, up to 50% of ocular MMP cases do not meet the immunopathological criteria. In addition, the risk of exacerbating conjunctival cicatrization makes ocular biopsy technically difficult to obtain ...
Andrea Gabusi +6 more
wiley +1 more source
Clinical Relevance of Autoantibodies in Patients with Autoimmune Bullous Dermatosis
Clinical and Developmental Immunology, 2012 The authors present their experience related to the diagnosis, treatment, and followup of 431 patients with bullous pemphigoid, 14 patients with juvenile bullous pemphigoid, and 273 patients with pemphigus.
Lilla Mihályi +4 more
doaj +1 more source
Autoimmuunsed villilised haigused [PDF]
, 2006 Villiliste haiguste rühma patogeneetiliseks aluseks on autoantikehade tekkimine epi der mise või dermoepidermaalse ühendusjoone normaalsete komponentide vastu. Kuigi hai gu sed erinevad omavahel haigete keskmise vanuse, kliinilise pildi ja histoloogilise
Kaur, Sirje, Pärna, Ene
core +2 more sources
Granulomatous Panniculitis in a Patient Treated With Cemiplimab: Case Report and Literature Review
JEADV Clinical Practice, EarlyView.ABSTRACT Immune checkpoint inhibitors (ICIs) have become a cornerstone in the treatment of advanced malignancies by enhancing antitumor immunity, but they may also trigger a broad spectrum of immune‐related adverse events (irAEs) involving multiple organs.
B. Lada‐Colunga +6 more
wiley +1 more source
Pemphigoid vegetans in childhood: A case report and short review of literature
Indian Journal of Dermatology, 2015 Pemphigoid vegetans is a very rare type of bullous pemphigoid which usually affects the elderly and has not been reported in children. It shows a clinical resemblance to pemphigus vegetans but has distinct histological and immunopathological features of ...
Yasmeen Khatib +3 more
doaj +1 more source