Chronic Morel‐Lavallée Lesion in a Pediatric Competitive Dancer: A Case Report and Literature Review
ABSTRACT Morel‐Lavallée lesions (MLLs) are rare internal degloving injuries resulting from shearing trauma, with few reported cases in the pediatric population. We present the case of a 16‐year‐old female competitive dancer with persistent right knee pain, skin atrophy, and ecchymosis after trauma sustained during a national dance competition, with MRI
Cameron Coakes +3 more
wiley +1 more source
Clinical Images: Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome presenting as aseptic pustular dermatosis: A rare clinical manifestation. [PDF]
Chen P +6 more
europepmc +1 more source
TNF Inhibitor Therapy in Corticosteroid‐Resistant or ‐Dependent Pediatric Neutrophilic Dermatosis
ABSTRACT Neutrophilic dermatoses are rare in children. Systemic corticosteroids are the first‐line treatment, but guidelines for second‐line therapies are lacking. We report five cases of children with systemic steroid‐resistant/dependent neutrophilic dermatoses, successfully treated with tumor necrosis factor inhibitors.
Laure Chêne +7 more
wiley +1 more source
Interleukin (IL)-17A Inhibitor as a Treatment for Darier Disease in the Pediatric Population. [PDF]
Barajas Mendez BD +4 more
europepmc +1 more source
Association of a Genetic Risk Score With Body Mass Index [PDF]
Davey Smith, George +2 more
core +2 more sources
Prescribing Patterns in Pediatric Hidradenitis Suppurativa
ABSTRACT Hidradenitis suppurativa (HS) is an inflammatory skin condition increasingly diagnosed in pediatric populations; however, data on treatment practices in this group remains limited. In this retrospective study of 163 patients diagnosed with HS ≤ 18 years of age, we found that treatment patterns varied significantly by disease severity.
Hannah Neimy +3 more
wiley +1 more source
[Wells Syndrome: Clinical Presentation and Literature Review]. [PDF]
Vega-Del Pilar YX +4 more
europepmc +1 more source
NEMO‐NDAS: Case Report and Review of the Literature
ABSTRACT NEMO‐deleted exon 5 autoinflammatory syndrome (NEMO‐NDAS) is the result of a gain‐of‐function IKBKG pathogenic variant leading to dysregulated NF‐κB signaling and systemic inflammation. We present a case of NEMO‐NDAS in a 2‐year‐old female presenting with recurrent fevers, subcutaneous nodules, lymphadenopathy, and splenomegaly.
Angela Yang +5 more
wiley +1 more source
Linear IgA Bullous Dermatosis in an Elderly Patient Following Meloxicam and Candesartan Use: A Case Report. [PDF]
Albyali S +6 more
europepmc +1 more source
Indices of systemic immunity in patients with eczema of dermatosis different clinikal course [PDF]
core

