Results 91 to 100 of about 1,536 (210)

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

Pathophysiological Mechanisms in Sclerosing Skin Diseases

Frontiers in Medicine, 2017
Sclerosing skin diseases represent a large number of distinct disease entities, which include systemic sclerosis, localized scleroderma, and scleredema adultorum.
Beate Eckes, Fang Wang, Pia Moinzadeh, Nicolas Hunzelmann, Thomas Krieg, Thomas Krieg, Thomas Krieg   +6 more
doaj   +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

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  

AB1852 DERMATO-NEURO SYNDROME PRECIPITATED BY COVID-19 INFECTION IN THE SETTING OF SCLEROMYXEDEMA [PDF]

, 2023
Catherine Grace Hobayan, Jody L. Lin
openalex   +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

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: A Complete Response to Prednisone [PDF]

, 1999
Daniel Rayson, John A. Lust, Alan J. Duncan, W.P. Daniel Su   +3 more
openalex   +1 more source

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

Liszaj śluzowaty z towarzyszącym zespołem Sjögrena [PDF]

, 2016
Lichen myxedematosus belongs to the group of disorders with the deposition of mucins in the skin. The disease may coexist with monoclonal gammapathy, e.g. myeloma multiplex or Waldenström macroglobulinemia.
Gruber, Joanna, Gruber-Szydło, Katarzyna, Maj, Joanna, Mędrek, Karolina, Reich, Adam, Wróbel, Tomasz   +5 more
core   +1 more source