Results 11 to 20 of about 207 (118)
Morphea Profunda Presenting As a Neuromuscular Mimic [PDF]
Abstract Localized scleroderma is characterized by idiopathic fibrosis of the skin and adjacent structures, and muscle involvement occurs predominantly in deep morphea. We report a patient with linear scleroderma who presented with slowly progressive atrophy, muscle weakness, and loss of function of her right arm ...
Voermans, N.C. +5 more
openaire +3 more sources
A 9‐year‐old child with painful nodules on the leg
Pediatric Dermatology, Volume 40, Issue 4, Page 730-732, July/August 2023.
Alma Nunzia Olivieri +2 more
wiley +1 more source
Radiation‐induced morphea – a rare, but not to be dismissed, adverse effect of radiotherapy
Dermatologic Therapy, Volume 34, Issue 5, September/October 2021.
Thilo Gambichler +2 more
wiley +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 19, Issue 8, Page 1236-1247, August 2021.
Margitta Worm +15 more
wiley +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 19, Issue 8, Page 1236-1248, August 2021.
Margitta Worm +15 more
wiley +1 more source
Localized morphea profunda: An atypical presentation
Morphea profunda is a variant of localized scleroderma, in which inflammation and sclerosis are found in the deep dermis, panniculus, fascia, or superficial muscle. It generally presents as diffuse, taut, and thickened skin, which is bound to the underlying tissue.
Arunima Dhabal +3 more
openaire +1 more source
Correspondence: The association between morphea profunda and monoclonal gammopathy: A case series [PDF]
It is known that eosinophilic fasciitis can be associated with monoclonal gammopathy. There is clinical similarity between eosinophilic fasciitis and morphea profunda, but it is unclear whether morphea profunda might be associated with monoclonal gammopathy.
Endo, Justin +6 more
openaire +3 more sources
Capsule SummaryLupus erythematosus panniculitis (LEP) is a rare variant of cutaneous lupus erythematosus. There are two case reports to date in the literature of LEP potentially triggered by anti‐TNFa therapies. Clinically, it is characterized by tender, erythematous subcutaneous indurated nodules or plaques on fatty body areas.
Cristina Grechin +4 more
wiley +1 more source
Morphea profunda is a rare disease that mainly affects young women and often has a progressive course with physical and psychological sequelae. The skin becomes sclerotic after an initial inflammatory reaction and joint contractures can develop. The aetiology is unknown. Until now, no successful therapy has been proven for this morphea variant.
Stausbøl-Grøn, Birgitte +3 more
openaire +3 more sources

