Results 61 to 70 of about 562 (139)

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, Nicholas Seng-Geok Goh, Ding Yuan Wang   +2 more
doaj   +1 more source

Dwa przypadki scleromyxedema

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, Maria Błaszczyk, Anna Kozłowska, Olga Glińska, Bartłomiej Kwiek, Agnieszka Terlikowska-Brzósko, Wojciech Sachs   +6 more
doaj  

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

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

Ultrastructural changes in scleromyxedema

Acta Dermato-Venereologica, 1975
Skin biopsy specimens from a 60-year-old patient with paraproteinemia and generalized changes of the skin typical of scleromyxedema were studied with the electron microscope. The dermis was dominated by collagen fibrils and accumulations of peculiar connective tissue cells, while elastic tissue was sparse and in some areas completely absent.
L, Danielsen, T, Kobayasi
openaire   +2 more sources

Treatment of scleromyxedema Arndt-Gottron with a novel intravenous immunoglobulin preparation

Dermatology Reports
Dear Editor, Scleromyxedema is known as a rare, severe mucinosis with characteristic waxy skin papules along with sclerodermiform induration of the skin and rare systemic manifestations. Monoclonal gammopathy of undetermined significance (MGUS; mostly
Niklas Negele, Julia K. Winkler, Alexander H. Enk   +2 more
doaj   +1 more source

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: A rare case report

Journal of Integrative Medicine and Research
Scleromyxedema (SM), or Arndt–Gottron disease, is a rare variant of lichen myxedematosus commonly associated with monoclonal gammopathy and may involve multiple organ systems.
Talluru Vani, Gudivada Saiteja, G.Varthini Rithika, Talamala Sampath Priya kumar   +3 more
doaj   +1 more source

Scleromyxedema

Indian Journal of Dermatology, Venereology, and Leprology, 2016
Ying, Yang, Hao, Chen, Wei, Zhang, Jian-Fang, Sun   +3 more
openaire   +3 more sources

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