Results 81 to 90 of about 848 (166)

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

Combination Oral Prednisone and Intravenous Immunoglobulin in the Treatment of Scleromyxedema

, 2005
Background: Scleromyxedema is a clinical variant of the rare disease papular mucinosis that has both cutaneous and systemic manifestations. Treatment options are numerous and tend to be associated with serious potential side effects and frequent relapse.
Marlene Dytoc, Parbeer Grewal, Candace Majeski, Muba Taher, Gilles Lauzon   +4 more
core   +1 more source

Scleromyxedema and inflammatory myopathy: A clinicopathology study of three patients

, 1986
Scleromyxedema (lichen myxedematosus is a rare cutaneous manifestation in patients with idiopathic inflammatory myopathy. The clinical and histological findings in three patients with this association are presented. Two patients had a severe inflammatory
Mastaglia, F.L., Cheah, P.S., Zilko, P.J., Ojeda, V.J., Harvey, J.M.   +4 more
core  

Suspected cardiac toxicity to intravenous immunoglobulin used for treatment of scleromyxedema

, 2008
Scleromyxedema is a rare, generalized form of lichen myxedematosus, which may be associated with systemic involvement and can be fatal. The therapeutic options available provide partial or inconsistent response and are associated with significant adverse
Binitha, M.P., Nandakumar, G., MP Binitha, Thomas, Daisy, Daisy Thomas, G Nandakumar   +5 more
core   +1 more source

Autologous stem cell transplantation in a patient with scleromyxedema

eJHaem, 2022
Sunita Nathan, Celalettin Ustun
doaj   +1 more source

Plasmapheresis in a patient with scleromyxedema.

, 1987
We describe a patient with progressive scleromyxedema who failed to respond to previously described treatment modalities. A trial of plasmapheresis was initiated, but after an initial promising response, his disease continued to progress.
Lookingbill, D P, Westheim, A I
core   +1 more source

Mimics of scleroderma

Indian Journal of Rheumatology, 2017
Systemic sclerosis is a rare autoimmune connective tissue disorder characterised typically by tightening and tethering of skin. However, several other disorders are also characterised by hardening and thickening of skin.
Kaveri K Nalianda, Mithun M Rathen, Soumya Jagadeesan, D Padmanabha Shenoy   +3 more
doaj  

An unusual case of granulomatous scleromyxedema

JAAD Case Reports, 2022
Lauren Michelle, BA, Sara Sabeti, BS, Katerina Yale, MD, Brittany Urso, MD, Bonnie Lee, MD, Janellen Smith, MD   +5 more
doaj   +1 more source

Treatment of recalcitrant scleromyxedema with thalidomide in 3 patients.

, 2004
Scleromyxedema is a generalized, papular, and sclerodermoid form of lichen myxedematosus associated with monoclonal gammopathy and systemic changes.
GIROLOMONI, Giampiero, Gubinelli E, Cocuroccia B, GISONDI, Paolo, Jorizzo JL, Sansbury JC   +5 more
core