Results 71 to 80 of about 1,053 (167)
S2k guideline: Diagnosis and therapy of localized scleroderma
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter +12 more
wiley +1 more source
A rare case of acral persistent papular mucinosis
Clinical Case Reports, 2020 In patients with asymptomatic papules of hands and feet, a clinical differential of acral persistent papular mucinosis should be thought of.
Joseph Jia‐Hong Toh +2 more
doaj +1 more source
Склеромикседема Арндта — Готтрона [PDF]
, 2012 The authors present a literature review and a case study of a rare form of dermatitis in a female patient aged 44 — Arndt — Gottron scleromyxedema associated with Ig-kappa monoclonal hyper-production. The authors also present the latest information about
CHIKIN V.V. +7 more
core +2 more sources
Pathophysiological Mechanisms in Sclerosing Skin Diseases
Frontiers in Medicine, 2017 Sclerosing skin diseases represent a large number of distinct disease entities, which include systemic sclerosis, localized scleroderma, and scleredema adultorum.
Beate Eckes +6 more
doaj +1 more source
Reticular erythematous mucinosis: A rare cutaneous mucinosis [PDF]
, 2019 Reticular erythematous mucinosis (REM) is a rare form of primary cutaneous mucinosis, most often involving the midline of the upper chest or back in middle-aged women. REM bears clinical and histopathologic resemblance to lupus erythematosus tumidus (LET)
Amer Ali Almohssen +2 more
core +1 more source
Dermoscopy and Reflectance Confocal Microscopy for the Diagnosis of Scleromyxedema [PDF]
, 2019 info:eu-repo/semantics ...
Borges, AS +3 more
core +2 more sources
Przegląd Dermatologiczny, 2011 Wprowadzenie: Scleromyxedema jest przewlekłą chorobą zaliczaną domucynoz. Kryteria jej rozpoznania to: charakterystyczne twardzinopodobnezmiany skórne, gammopatia monoklonalna bez współistniejącychzaburzeń funkcji tarczycy, awbadaniu histopatologicznym ...
Jadwiga Dwilewicz-Trojaczek +6 more
doaj
NFκB activation and stimulation of chemokine production in normal human macrophages by the gadolinium-based magnetic resonance contrast agent Omniscan: possible role in the pathogenesis of nephrogenic systemic fibrosis. [PDF]
, 2010 OBJECTIVE: Nephrogenic systemic fibrosis (NSF) is a generalised fibrotic disorder occurring in certain individuals with renal insufficiency exposed to gadolinium-based contrast agents (GdBCA) for MRI.
Addya, Sankar +4 more
core +1 more source
Scleromyxedema with systemic involvement mimics rheumatic diseases [PDF]
, 1986 Scleromyxedema is an infiltrative skin disease produced by hyaluronic acid deposition in the dermis. A benign monoclonal gammopathy is usually present. We report 2 patients with scleromyxedema and systemic illnesses.
Chanda +14 more
core +1 more source