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
High-Dose Intravenous Immunoglobulin in Skin Autoimmune Disease
Frontiers in Immunology, 2019 The immunomodulatory potential and low incidence of severe side effects of high-dose intravenous immunoglobulin (IVIg) treatment led to its successful application in a variety of dermatological autoimmune diseases over the last two decades.
Jochen H. O. Hoffmann, Alexander H. Enk
doaj +1 more source
Clinicopathologic Correlation: Differentiating Between Localized Lichen Myxedematosus and Scleromyxedema [PDF]
, 2022 Kamran Harper +3 more
openalex +1 more source
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
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
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 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
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
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