Results 61 to 70 of about 1,700 (160)
Biomarkers in skin autoimmunity—An update on localised scleroderma
Skin Health and Disease, Volume 4, Issue 2, April 2024.Newest research on biomarkers in localised scleroderma reviewed. Abstract Human autoimmune diseases are complex and highly diverse conditions that can be of localised or systemic nature. Understanding the basic biology of autoimmune diseases goes hand in hand with providing the clinics with valuable biomarkers for managing these diseases.
Adrián Hernández‐Bustos +2 more
wiley +1 more source
Scleroderma mimics – Clinical features and management [PDF]
, 2020 Systemic sclerosis is a severe immune-mediated rheumatic disease by virtue of its clinical impact and mortality. There are a number of other sclerosing skin diseases that should be considered in the differential diagnosis and these are important because ...
Denton, CP, Ong, VH, Orteu, CH
core
Scleromyxedema (Arndt - Gottron Syndrome) Developing Under Tenofovir Treatment for Hepatitis B: Unique Presentation in a Bulgarian Patient! [PDF]
, 2019 BACKGROUND: Scleromyxedema, also referred to as the Arndt-Gottron (S-AG) syndrome or the systemic form of Lichen myxedematosus (LM), is a cutaneous mucinosis with a chronic course and high lethality from systemic involvement of other organs and systems ...
Patterson, James +2 more
core +3 more sources
Nephrogenic systemic fibrosis associated with stromal and vascular calcification, report of two cases [PDF]
, 2009 Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75035/1/j.1600-0560.2008.01205.x ...
Alegre, Maria-Luisa +10 more
core +1 more source
Discrete papular lichen myxedematosus: a rare entity or an under- diagnosed disease? [PDF]
, 2016 Primary cutaneous mucinoses are characterized by abnormal mucin deposits in the skin. Discrete papular lichenmyxedematosus (DPLM) is an unusual subtype which is characterized by the presence of multiples smooth, waxy, or flesh-colored papules, 2 to 5 mm
Gallouj, Salim +3 more
core +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
Description of twelve cases of nephrogenic fibrosing dermopathy and review of the literature
, 2006 Objectives: To review the clinical and laboratory features of twelve cases of nephrogenic fibrosing dermopathy (NFD) studied at our institution and of 70 previously described cases in the literature. Methods: Clinical evaluation and laboratory studies
Artlett, Carol M. +5 more
core +2 more sources
Indian journal of dermatology, venereology and leprology, 2017 Scleromyxedema was observed in a 43 year old male.The lesions were shiny, waxy-looking, soft,, papules, 2 to 4 mm in diameter and were most marked on the neck and ear lobules. There was no evidence of paraproteinemia.
A K, Bajaj +3 more
openaire +1 more source
JEADV Clinical Practice, Volume 3, Issue 4, Page 1294-1297, September 2024.
Emily R. Gordon +7 more
wiley +1 more source
Scleromyxedema: An Atypical Case
Indian Journal of Dermatology, 2015 Scleromyxedema is a rare, chronic and persistent idiopathic disorder characterized by a generalized papular eruption due to dermal mucin deposition with an increase in dermal collagen. Patients usually have associated paraproteinemia. We describe the case of a 59-year-old gentleman with features of scleromyxedema, who had severe pruritus, scalp ...
Emy Thomas +3 more
openaire +3 more sources