Results 11 to 20 of about 7,109,345 (167)

Pênfigo vegetante induzido por uso de enalapril Pemphigus vegetans induced by use of enalapril [PDF]

Anais Brasileiros de Dermatologia, 2011
Pênfigo Vegetante foi primeiramente descrito como uma variante do pênfigo vulgar, em 1876, por Neumann. Em 1889, Hallopeau descreveu um paciente com pústulas e placas vegetantes, e sugeriu ser uma variante do Pênfigo Vegetante de Neumann.
André Ricardo Adriano, Antonio Gomes Neto, Gustavo R Hamester, Daniel H Nunes, Gabriella Di Giunta   +4 more
doaj   +3 more sources

Pemphigus vegetans: surgical approach as a complementary treatment [PDF]

Surgical & Cosmetic Dermatology, 2022
Pemphigus vegetans is considered a rare clinical variant of Pemphigus vulgaris and is associated with recurrent lesions that can evolve into extensive vegetative plaques that are difficult to resolve.
João Felipe Rossival-Preto, Ingrid Stresser-Gioppo, Flávia Fajardo, Marina Carrara-Camilo-Barbosa, Ivander Bastazini-Junior   +4 more
doaj   +2 more sources

Pemphigus vegetans of hallopeau

Indian Journal of Dermatology, 2005
A 42 year old male had pemphigus vegetans of Hallopeau of groin and perianal area for the last 4 months. He also had lesions on scalp and mouth. Histology showed intraepidermal eosinophilic abscess.
Nanda Soni, Grover Chander, Garg Vijay, Reddy B   +3 more
doaj   +1 more source

Pustular psoriasis: pathophysiology and current treatment perspectives

Psoriasis: Targets and Therapy, 2016
Katie E Benjegerdes,1 Kimberly Hyde,2 Dario Kivelevitch,3 Bobbak Mansouri1,4 1Texas A&M Health Science Center College of Medicine, Temple, 2Texas A&M Health Science Center College of Medicine, Round Rock, 3Division of Dermatology, Baylor ...
Benjegerdes KE, Hyde K, Kivelevitch D, Mansouri B   +3 more
doaj   +1 more source

Epidermolysis Bullosa Classification and Current Approach to Diagnosis. [PDF]

Pediatr Dermatol
ABSTRACT Epidermolysis bullosa (EB) is a heterogeneous group of rare genodermatoses marked by skin fragility and bullae formation induced by minor trauma. Pathologic variants in at least 21 genes are associated with EB, grouped into four major subtypes based predominantly on the plane of cleavage within the skin.
Mumber HE, Perman MJ.
europepmc   +2 more sources

Novel COL7A1 Mutations of Hallopeau-Siemens Type Recessive Dystrophic Epidermolysis [PDF]

Novel COL7A1 Mutations of Hallopeau-Siemens Type Recessive Dystrophic Epidermolysis
application/pdf Dystrophic epidermolysis bullosa (DEB) is caused by mutations in the COL7A] gene encoding type VII collagen. DEB is clinically characterized by mucocutaneous blistering in response to minor trauma. followed by scarring and nail dystrophy. DEB is inherited in either an autosomal dominant (DDEB) or recessive (RDEB) fashion. DDEB basically
Murai, Takaya, Nakano, Hajime, Hashimoto, Isao, Sawamura, Daisuke, Tamai, Katsuto, Hanada, Katsumi   +5 more
core   +3 more sources

Non-FDA-Approved Uses of Apremilast in Dermatology: A Review of Current Available literature

Nepal Journal of Dermatology, Venereology & Leprology, 2022
Introduction: Apremilast, an oral phosphodiesterase-4 inhibitor, decreases the production of pro-inflammatory cytokines including tumour necrosis factor-α, interleukin-12/23, IL-12, IL-2, and interferon-γ; while upregulating the anti-inflammatory ...
Saurabh Bhatia
doaj   +3 more sources

Palmoplantar pustulosis: pathogenesis, differential diagnosis, and treatment. [PDF]

J Dtsch Dermatol Ges
Summary Palmoplantar pustulosis (PPP) is a chronic inflammatory and often painful disease characterized by sterile pustules on the palms and soles, significantly impairing quality of life. Women are more frequently affected than men, and smoking is a major trigger. Under biologic therapies, especially TNF antagonists, a paradoxical PPP may occur.
Mössner R, Fetter T, Sabat R, Mrowietz U, Cramer N, Wilsmann-Theis D.   +5 more
europepmc   +2 more sources

Hallopeau-Type Pemphigus Vegetans Emerging Under Long-Term Oral Prednisone Therapy

Dermatology Review
Azzahra Siregar, Otto Ahvonen, Madina Shahmarova, Maja Kleniewska, Agnieszka Markiewicz, Agnieszka Owczarczyk-Saczonek   +5 more
openaire   +3 more sources

Narrowing the Differential: A Unique Case of Dystrophic Epidermolysis Bullosa. [PDF]

Case Rep Pediatr
Dystrophic epidermolysis bullosa (DEB) is a rare inherited skin disorder characterized by mechanical stress‐induced blistering and skin erosion. Diagnosis is confirmed through molecular genetic testing, typically identifying mutations in the COL7A1 gene. DEB can mimic other neonatal dermatologic conditions, making early identification challenging.
Yacobucci L, Edwards C, Oosbree AV, Newman R.   +3 more
europepmc   +2 more sources