Results 41 to 50 of about 16,051 (234)

Linear atrophoderma of Moulin: a case report and review of the literature

Dermatology Practical & Conceptual, 2013
Linear atrophoderma of Moulin is a rare, acquired, linear dermatosis. We present a 17-year-old girl with multiple asymptomatic brownish atrophic plaques in a zosteriform distribution on the left side of the trunk.
Aikaterini Patsatsi, Aikaterini Kyriakou, George Chaidemenos, Dimitrios Sotiriadis   +3 more
doaj   +1 more source

Optimal management strategies for paediatric morphea – insights from a case series

Pediatria Polska
Juvenile localized scleroderma, or morphea, is a rare chronic inflammatory disease primarily affecting the skin and subcutaneous tissue. Treatment options for paediatric cases are diverse, with a lack of standardised guidelines.
Kinga Łagosz, Natalia Bień, Justyna Ceryn, Paulina Barsińska, Dorota Sobolewska-Sztychny, Joanna Narbutt, Aleksandra Lesiak   +6 more
doaj   +1 more source

Morphea “en coup de sabre”: an unusual oral presentation [PDF]

, 2017
Morphea, or localized scleroderma, is an inflammatory disease that leads to sclerosis of the skin and underlying tissues due to excessive collagen deposition.
Esguep, Alfredo, Martínez, René, Marín, Constanza, Niklander, Sven   +3 more
core   +1 more source

En coup de sabre morphea: An uncommon condition in Africa

Dermatology Reports, 2022
The term en coup de sabre morphea refers to a lesion of linear morphea typically located in the frontoparietal scalp and/or the paramedian forehead, often resembling a strike with a sword.
Lehlohonolo Makhakhe, Ncoza Dlova, Annette Smith, Michelle du Preez   +3 more
doaj   +1 more source

Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts. [PDF]

, 2017
ObjectiveTo compare faecal microbial composition in patients with systemic sclerosis (SSc) from 2 independent cohorts with controls and to determine whether certain genera are associated with SSc-gastrointestinal tract (GIT) symptoms.DesignAdult patients
Braun, Jonathan, Chang, Lin, Chang, Yu-Ling, Clements, Philip J, Hoffmann-Vold, Anna-Maria, Hov, Johannes R, Jacobs, Jonathan P, Kummen, Martin, Labus, Jennifer S, Lagishetty, Venu, Mayer, Emeran A, Midtvedt, Øyvind, Molberg, Øyvind, Tillisch, Kirsten, Volkmann, Elizabeth R   +14 more
core   +1 more source

Pansclerotic Morphea with Features of Eosinophilic Fasciitis: Distinct Entities or Part of a Continuum? [PDF]

, 2014
Scleroderma is a highly complex disorder in its clinical manifestations and pathogenesis. It has a wide range of clinical manifestations due to varying degrees of vasculopathy, autoimmunity, altered endothelium function, and abnormal fibrosis.
Canty, Kristi, Hoeltzel, Mark F., Odhav, Ashika   +2 more
core   +1 more source

Parry–Romberg syndrome associated with en coup de sabre in a patient from South Sudan – a rare entity from East Africa: a case report

Journal of Medical Case Reports, 2019
Background Parry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. It is usually slowly progressive, occurring more in females, and affects primarily one side
Jimmy Girgis William Abdelnour, Youeil Girgis William Abdelnour, Rose-Mery Amin Boushra Kerollos, Ziryab Imad Taha Mahmoud   +3 more
doaj   +1 more source

LINEAR SCLERODERMA WITH SEVERE LEG DEFORMITY

Australasian Journal of Dermatology, 1992
SummaryLinear scleroderma is an unusual form of localised scleroderma, mainly affecting the legs and occurring primarily in children. Sometimes the linear lesions may extend to involve the underlying muscles and bones, with severe disturbances in growth and possibly flexion deformities of the legs.1,2,3,4 In this study, two cases suffering from linear ...
Hatzis, J.A., Stratigos, A.J., Dimopoulos, J.Ch., Tzermias, C.K., Orfanidou, A., Bassioukas, K.Ch.   +5 more
openaire   +4 more sources

Capillaroscopy in 2016 : new perspectives in systemic sclerosis [PDF]

, 2016
Systemic sclerosis (SSc) is an autoimmune disorder of unknown etiology characterized by early impairment of the microvascular system. Nailfold microangiopathy and decreased peripheral blood perfusion are typical clinical aspects of SSc.
Cutolo, M, Llado, A, Paolino, S, Pizzorni, C, Ruaro, B, Smith, Vanessa, Sulli, A   +6 more
core   +1 more source

Multimodal optical diagnostics of the microhaemodynamics in upper and lower limbs [PDF]

, 2019
The introduction of optical non-invasive diagnostic methods into clinical practice can substantially advance in the detection of early microcirculatory disorders in patients with different diseases.
Dremin, Viktor V., Dunaev, Andrey V., Goltsov, Alexey, Makovik, Irina N., Rafailov, Edik U., Sokolovski, Sergei G., Zherebtsov, Evgeny A., Zherebtsova, Angelina I.   +7 more
core   +4 more sources