Results 41 to 50 of about 2,694 (176)

Mycosis Fungoides in Pediatric Patients Revealed by Recalcitrant Psoriasiform Palmoplantar Keratoderma

JEADV Clinical Practice, EarlyView.
ABSTRACT Mycosis fungoides is a cutaneous T‐cell lymphoma with a classically relatively good prognosis, mostly diagnosed in men over the age of 50. It classically manifests as erythematosquamous plaques, but can take a variety of forms. Here we describe four cases of mycosis fungoides diagnosed in children, with psoriasiform palmoplantar keratoderma as
S. Grandjacquot, C. Ram‐Wolff, A. De Masson, P. Drabent, S. Fraitag, P. Bataille, M. Battistella, E. Bourrat   +7 more
wiley   +1 more source

Folliculitis decalvans: the use of dermatoscopy as an auxiliary tool in clinical diagnosis [PDF]

Anais Brasileiros de Dermatologia, 2013
Folliculitis decalvans is an inflammatory presentation of cicatrizing alopecia characterized by inflammatory perifollicular papules and pustules. It generally occurs in adult males, predominantly involving the vertex and occipital areas of the scalp. The
Mariana Rocha Fabris, Clarisse Pereira Melo, Daniel Fernandes Melo   +2 more
doaj   +1 more source

Sterile Nasal Septal Abscess in Ulcerative Colitis With Crypt Abscess‐Like Neutrophilic Infiltration

The Laryngoscope, EarlyView.
We report a rare case of sterile nasal septal abscess in a patient with ulcerative colitis. Histopathological analysis revealed crypt abscess‐like neutrophilic infiltration in the nasal mucosal glands, resembling a typical feature of ulcerative colitis.
Masakazu Murayama, Yoshihito Tanaka, Tomoyuki Yokose, Toshikazu Shimane   +3 more
wiley   +1 more source

Case for diagnosis. A bluish nodule on the scalp [PDF]

Anais Brasileiros de Dermatologia, 2017
: Acrospiroma, also known as hidradenoma, is a rare cutaneous tumor that has several histological characteristics. As a consequence, a high index of suspicion is necessary for its diagnosis. Here we report a case that illustrates the importance of a good
Sylvia Aide Martinez-Cabriales, Ivette Miranda-Maldonado, Jorge Ocampo-Candiani   +2 more
doaj   +1 more source

Trichophyton mentagrophytes type VII: cohort study on patient characteristics, clinical features, disease course, and treatment

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives Sexually transmitted infections with Trichophyton mentagrophytes type VII (TMVII) have been reported in several countries. The aim of our study was to identify epidemiological and clinical features in order to improve prevention, diagnosis, and treatment.
Konstanze Kämmerer, Julia Huynh, Cornelia Deutsch, Stefanie May, Sertac Uyar, Alexander Nast, Christoph Zeyen, Ricardo Niklas Werner   +7 more
wiley   +1 more source

Nurse‐Led Models of Service Delivery for Skin Cancer Detection: A Systematic Review

Journal of Advanced Nursing, EarlyView.
ABSTRACT Aim To consolidate evidence on nurse‐led models for skin cancer detection by focusing on their roles, comparing their effectiveness to physician‐led care and highlighting any value‐added benefits. Design Systematic review methodology with narrative synthesis. Data Sources MEDLINE Complete, PubMed, Embase, CINAHL Complete, ScienceDirect, Scopus,
Leila Kattach, Heidi Singleton, Steven Ersser, Debbie Holley, Ian Pearson, Abdulrahman Shadeed   +5 more
wiley   +1 more source

Demodicosis as treatment complication of amicrobial pustulosis of the folds [PDF]

Anais Brasileiros de Dermatologia, 2018
: Amicrobial pustulosis of the folds is a chronic relapsing neutrophilic dermatosis characterized by sterile pustules compromising skin folds, scalp, face and periorificial regions. It predominantly affects women.
Marilia Formentini Scotton Jorge, Lívia Maria Zanardi Miguel, Cíntia Santos Braghiroli, Juliano Vilaverde Schmitt   +3 more
doaj   +2 more sources

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Erosive pustular dermatosis of the scalp - is it really a rare condition? [PDF]

Vojnosanitetski Pregled, 2014
Introduction. Erosive pustular dermatosis of the scalp (EPDS) is a rare disorder of unknown etiology that usually occurs in the elderly and is characterized by multiple pustules, erosions and crusts that appear on the scalp leading to scarring ...
Levakov Olivera, Gajić Branislava
doaj   +1 more source

Efficacy and Safety of Topical Dapsone in Dermatology: A Scoping Review of Clinical Studies

Journal of Cosmetic Dermatology, Volume 24, Issue 10, October 2025.
ABSTRACT Background Dapsone (4,4′‐Diamino diphenyl sulfone) has been utilized in managing a wide variety of mucocutaneous conditions, usually as a systemic product. Topical dapsone is commercially available as 5% and 7.5% gel and is FDA‐approved for acne vulgaris.
Bahareh Abtahi‐Naeini, Hossein Sattari, Kimia Afshar, Fereshte Rastegarnasab, Mahsa Pourmahdi‐Boroujeni   +4 more
wiley   +1 more source