Results 81 to 90 of about 1,053 (167)

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, Hadj, Iman, Mernissi, Fatima Zahra, Meziane, Mariame   +3 more
core   +1 more source

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, Curran, James J., Gregg, Kevin, Krausz, Thomas, Levine, Jerrold S., Salgia, Reena, Shea, Christopher R., Song, Jie, Sweiss, Nadera J., Volkov, Suncica, Woodruff, James   +10 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  

Experiences of patients with cutaneous manifestations of monoclonal gammopathy of undetermined significance (MGUS): Insights from the first disease‐specific support group

JEADV Clinical Practice, Volume 3, Issue 4, Page 1294-1297, September 2024.
Emily R. Gordon, Caroline Chen, Oluwaseyi Adeuyan, Brigit A. Lapolla, Megan H. Trager, Celine M. Schreidah, Lauren M. Fahmy, Larisa J. Geskin   +7 more
wiley   +1 more source

Scleromyxedema.

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, S C, Gupta, A, Tripathi, P A, Singh   +3 more
openaire   +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., Jimenez, Sergio A., Latinis, Kevin, Mendoza, Fabian A., Piera-Velazquez, Sonoles, Sandorfi, Nora   +5 more
core   +2 more sources

Atypical scleromyxedema presenting with cutaneous and cardiovascular manifestations

International Medical Case Reports Journal, 2016
Sue-Ann Teh,1 David A Kandiah2 1Department of Health Western Australia, Bunbury Hospital, Bunbury, 2School of Psychiatry and Clinical Neurosciences, Faculty of Medicine, Dentistry and Health Sciences, University of Western Australia, Crawley, WA ...
Teh SA, Kandiah DA
doaj  

Scleromyxedema Treated Successfully with Methotrexate

Journal of Clinical Rheumatology and Immunology
Background: Scleromyxedema is a rare, chronic cutaneous mucinosis of unknown etiology, characterized by widespread papular eruptions, dermal mucin deposition, fibroblast proliferation, and frequent systemic involvement.
Ravinash Ratnam, Jasmin Raja
doaj   +1 more source

SARS-CoV-2: A Potential Trigger of Dermato-Neuro Syndrome in a Patient with Scleromyxedema [PDF]

, 2021
Fesler, Mark, Fritz, Mike, Goldenberg, Linda, Hurley, M. Yadira, Morris, Gabriela M., Rukmangadachar, Lokesh, Tinker, Daniel, Wessel, Alex W.   +7 more
core   +2 more sources

Unusual variant of scleromyxedema presenting with severe systemic involvement and atypical adnexal proliferations – A histological pitfall with the risk of unnecessary surgeries

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 3, Page 434-437, March 2024.
Ines Bertlich, Mona Bidier, Tilman Schulz, Dmitry V. Kazakov, Eva M. C. Schwaibold, Wolfgang Hartschuh   +5 more
wiley   +1 more source