Results 71 to 80 of about 1,700 (160)
OA14 A case of scleromyxedema with muscle involvement including myotonia and dysphagia [PDF]
Rheumatol Adv Pract, 2022 Introduction/Background Scleromyxedema is a rare, para-neoplastic, progressive condition of the Lichen myxedematous family. It is clinically characterized by generalized papules with skin infiltration and underlying systemic disorders, which may be fatal
Marwa Mohareb, A. Ugwoke, N. Gendi
europepmc +2 more sources
SARS-CoV-2: A Potential Trigger of Dermato-Neuro Syndrome in a Patient with Scleromyxedema [PDF]
, 2021 Fesler, Mark +7 more
core +2 more sources
Acta Medica Iranica, 1996 Scleromyxedema is a rare, chronic, progressive, fibromucinous disorder of unknown etiology, characterized by lichenoid waxy papules and firm induration of skin of trunk, face, forearm and hands; fibroblast proliferation and mucin deposition in the upper dermis.
Z. Safaii Naraghi. +1 more
openaire +2 more sources
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 +5 more
core +1 more source
Extensive mucinous eccrine naevus following the lines of Blaschko: a new type of eccrine naevus [PDF]
, 2006 España, A. (Agustín) +2 more
core +1 more source
Non-healing painful ulcers in a patient with chronic kidney disease and role of sodium thiosulfate: a case report [PDF]
, 2008 Arshdeep Tindni +17 more
core +1 more source
Generalized scleroderma-like induration associated with D-penicillamine elastosis perforans serpiginosa in Wilson's disease [PDF]
, 2022 Agosta, Daniele +6 more
core +1 more source
Rapid Improvement of Scleromyxedema Associated With IgG Kappa Monoclonal Gammopathy After Intravenous Immunoglobulin (IVIG) [PDF]
, 2022 Kingsley, Jacob
core +1 more source