Results 61 to 70 of about 1,536 (210)

Monoclonal Gammopathy–Associated Scleromyxedema Presenting as Leonine Facies [PDF]

open access: yes, 2018
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/146383/1/art40530.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/146383/2/art40530_am ...
Khanna, Dinesh   +2 more
core   +1 more source

Adverse reactions to the injection of face and neck aesthetic filling materials:a systematic review [PDF]

open access: yes, 2023
Adverse reactions, caused during the inflammation and healing process, or even later, can be induced by the injection of dermal filler and can present a variety of clinical and histological characteristics.
Carvas, Janaína Badin   +7 more
core   +1 more source

A rare association of scleromyxedema with cutis verticis gyrata

open access: yesIndian Dermatology Online Journal, 2016
Cutis verticis gyrata (CVG) is characterized by redundant skin on the scalp that exhibits deep furrows and convolutions. We report a 58-year-old male who presented with multiple raised asymptomatic skin-colored lesions over the chest and abdomen and ...
Savita Koregol   +3 more
doaj   +1 more source

Letter on 'European dermatology forum S1-guideline on the diagnosis and treatment of sclerosing diseases of the skin, Part 2: Scleromyxedema, scleredema and nephrogenic systemic fibrosis' [PDF]

open access: yes, 2018
We read with interest the guidelines recently published on sclerosing diseases of the skin (Part 2: Scleromyxedema, scleredema and nephrogenic systemic fibrosis)[1, 2].
Blankestijn, Peter   +4 more
core   +2 more sources

Assessment of Treatment Response in Patients With Scleromyxedema by the Double Modified Rodnan Skin Score

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Background Scleromyxedema (SMX) is a cutaneous mucinosis characterised by an abnormal accumulation of mucin in the skin and limited treatment options. Assessment of therapy response during treatment is challenging. Objectives Patients with SMX receiving high‐dose intravenous IVIg therapy were included to assess validity of the double modified ...
Julia K. Winkler, Alexander H. Enk
wiley   +1 more source

Scleromyxedema with Subcutaneous Nodules: Successful Treatment with Thalidomide and Intravenous Immunoglobulin

open access: yesCase Reports in Dermatology, 2013
Scleromyxedema is a rare cutaneous mucinosis, usually presenting with generalized papular eruption and sclerodermoid induration, monoclonal gammopathy and systemic manifestations.
M. Dolenc-Voljč   +3 more
doaj   +1 more source

Scleromyxedema, a therapeutic dilemma

open access: yesIndian Journal of Dermatology, 2015
Scleromyxedema is characterized by indurated erythematous papules disseminated on the face, chest and limbs. About twenty cases treated with thalidomide, stem cells, melphalan and immunoglobulin with varying results have been described.
Julio Cesar Salas-Alanis   +3 more
doaj   +1 more source

Successful Treatment of Scleromyxedema with IVIG: A Case Report

open access: yesJournal of Mazandaran University of Medical Sciences, 2018
Scleromyxedema (SM), a rare progressive cutaneous mucinosis with a systemic involvement, presents with progressive dermal mucin depositions, causing skin thickening.
Fatemeh Niksolat   +5 more
doaj  

Systemic sclerosis without antinuclear antibodies or Raynaud's phenomenon: a multicentre study in the prospective EULAR Scleroderma Trials and Research (EUSTAR) database [PDF]

open access: yes, 2017
Objective. To assess patients with SSc who present without circulating ANAs or RP. Methods. Five thousand three hundred and ninety patients who fulfilled the ACR criteria for SSc and were enrolled in the EULAR Scleroderma Trials and Research (EUSTAR ...
Carreira, Patricia E.   +9 more
core  

Systemic Sclerosis Mimics [PDF]

open access: yes, 2019
Many clinical conditions are presenting with sclerosis of the skin and with tissue fibrosis. These conditions may be confused with systemic sclerosis (SSc, scleroderma).
Kodet, Ondřej, Oreská, Sabína
core   +2 more sources

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