Results 91 to 100 of about 35,808 (310)

Reversal of Canities in a Patient With Frontal Fibrosing Alopecia

JEADV Clinical Practice, EarlyView.
ABSTRACT Frontal fibrosing alopecia (FFA) is a primary lymphocytic cicatricial alopecia, most commonly affecting postmenopausal women, characterized by progressive frontotemporal hairline recession and eyebrow loss. Hair repigmentation (canities reversal) is an extremely rare event, especially in older individuals with long‐standing white hair.
Nicolò Rivetti
wiley   +1 more source

Comparison of personality traits among patients with psoriasis, atopic dermatitis, and stress: a pilot study

, 2020
Background: Psoriasis and atopic dermatitis are chronic skin diseases that greatly affect the quality of life. Both diseases can be triggered or exacerbated by stress. Objective: We aimed to differentiate personality traits between patients with chronic
Grine, Lynda, Hofbauer, Günther F. L., Lambert, Jo, Lapeere, Hilde, Maes, Nele, Tochtermann, Giulia, Vervaet, Myriam   +6 more
core   +1 more source

Successful Use of Bimekizumab in Refractory Acute Generalised Exanthematous Pustulosis Triggered by Amoxicillin‐Clavulanate

JEADV Clinical Practice, EarlyView.
ABSTRACT Acute generalised exanthematous pustulosis (AGEP) is a rare, acute neutrophilic dermatosis most commonly triggered by drugs, which typically resolves within 2 weeks following withdrawal of the causative agent. Topical and systemic corticosteroids remain the standard treatment.
Alexandra Junge, Charlotte Vogel, Theresa Hempel, Basil Signer, Nikhil Yawalkar, Kristine Heidemeyer   +5 more
wiley   +1 more source

Relatório dos projetos concluídos 2009. [PDF]

, 2015
bitstream/item/58245/1/doc138 ...
COLDEBELLA, A., SCHEUERMANN, G. N.
core  

New Biologic and Small Molecule Therapies for Hidradenitis Suppurativa

JEADV Clinical Practice, EarlyView.
ABSTRACT Hidradenitis suppurativa (HS) is an inflammatory skin disease that has historically been underdiagnosed and, until recently, under‐researched. Furthermore, the pathophysiology of HS is complex, and not fully understood. Just three biologic medications—adalimumab (anti‐TNF‐α), secukinumab (anti‐IL17A) and bimekizumab (anti‐IL17A/F) are licensed
Emily Pender, Rosalind Hughes, Brian Kirby   +2 more
wiley   +1 more source

Mask-related dermatological problems during COVID-19 pandemic among a sample of Egyptian population

Journal of the Egyptian Women’s Dermatologic Society
Background During the coronavirus disease 2019 pandemic, mask wearing was obligatory in many countries to decrease infection risk among individuals. However, long-term mask wearing was associated with the development of various adverse skin reactions ...
Ihab Younis, Sherine M. Elsabbagh, Samah E. Ibrahim   +2 more
doaj   +1 more source

Undermined and Overlooked: A Diagnostic Challenge in the Gluteal Cleft

JEADV Clinical Practice, EarlyView.
G. E. Beraja, Y. Dalia, J. A. Jaller
wiley   +1 more source

A Refractory Leg Skin Ulcer Associated With Multiple Myeloma Successfully Treated With Plasma Exchange, Lenalidomide, and Dexamethasone

JEADV Clinical Practice, EarlyView.
ABSTRACT Multiple myeloma (MM) is a malignant plasma cell disorder that primarily presents with CRAB symptoms (calcium elevation, renal failure, anemia, and bone abnormalities). In rare cases, MM manifests with systemic complications like skin ulcers, which present management challenges. Here, we report a 78‐year‐old Japanese man with MM and refractory
Naoko Hattori, Yutaka Kuwatsuka, Tomoka Waseda, Daisuke Ehara, Koji Ando, Hiroyuki Murota   +5 more
wiley   +1 more source

Blaschkoid Facial Lesion in an Adult Woman

JEADV Clinical Practice, EarlyView.
João Teixeira, Joana Xará, André Aparício‐Martins, José Carlos Cardoso, Margarida Gonçalo   +4 more
wiley   +1 more source

Juvenile Mycosis Fungoides: A Multicenter Retrospective Italian Study

JEADV Clinical Practice, EarlyView.
This multicenter retrospective study included 29 juvenile mycosis fungoides (JMF) patients from five Italian centres with confirmed histopathological diagnosis. most often presents with hypopigmented/classic variants and CD8+ phenotype. Early‐onset cases ( < 14 years) show better long‐term outcomes.
Andrea Michelerio, Gabriele Roccuzzo, Iria Neri, Alessandro Pileri, Alessandro Svizzero, Maria Beatrice De Felici Del Giudice, Vieri Grandi, Pietro Quaglino, Valeria Brazzelli   +8 more
wiley   +1 more source