Results 41 to 50 of about 3,110,367 (185)
Pansclerotic morphea: A case report
Generalized disabling pansclerotic morphea is a rare and mutilating form of morphea involving the dermis, subcutaneous tissue, fat, muscle, and even bone. It most often occurs in young children but adults can also be affected. We report a case of rapidly
Anum Sadia +3 more
core +1 more source
The localized scleroderma (morphea) is the clinical option of the juvenile scleroderma, the third in prevalence rheumatic condition in pediatrics. The article summarizes all the data on the classification, diagnostics, and differential diagnosis of ...
Rinat K. Raupov +2 more
doaj +1 more source
Reflectance Confocal Microscopy Applied to Linear (en Coup de Sabre) Morphea
En coup de sabre morphea is a clinical variant of morphea, presenting as a linear depressed, atrophic area in the paramedian forehead or the frontoparietal scalp, resembling a stroke from a sword.
Piccolo, Arianna +7 more
core +1 more source
Morphea After Liposuction Ultrasonography
Liposuction is a common aesthetic procedure; however, to date, liposuction has not been linked to morphea. The aim was to review cases with a history of liposuction that presented active morphea lesions in the same surgery regions and were confirmed by ...
Ximena Wortsman +9 more
core +1 more source
Questions raised by a case of adult-onset linear nodular scleroderma [PDF]
Morphea presenting clinically with nodular or keloidal skin changes is extremely rare. Nodular scleroderma or keloidal morphea presenting in a linear distribution is even more uncommon. We present an otherwise healthy young woman with unilateral, linear,
Marcelus, Christina +4 more
core +1 more source
Genomics and epigenomics of tissue repair: Implications for personalized medicine
Genomic and epigenomic mechanisms govern tissue repair and regeneration through dynamic regulation of inflammation, cell fate, and extracellular matrix remodeling. The integration of multi‐omics, artificial intelligence, and precision regenerative therapies enables biomarker‐driven, personalized approaches to enhance healing and minimize fibrosis ...
Jharna Medhi +7 more
wiley +1 more source
Parry-Romberg syndrome. Overlap with linear morphea
Parry-Romberg syndrome, also known as progressive hemifacial atrophy, was first described by Parry in 1825 then Romberg in 1846. It is a poorly understood rare disorder characterized by progressive hemifacial atrophy of the skin, subcutaneous tissue, and sometimes, the underlying structures including muscles, cartilages and bones.
Sultan, Al-Khenaizan, Lemmese, Al-Watban
openaire +2 more sources
Cutaneous lymphomas – an update
Primary cutaneous lymphomas and lymphoproliferative disorders are defined by integrated clinical, histopathological, immunophenotypic and genetic features as diagnostic criteria also in the 5th edition of the WHO classification of haematolymphoid tumors.
Werner Kempf, Christina Mitteldorf
wiley +1 more source
Treatment strategies for interstitial granulomatous dermatitis: Systematic review and expert opinion
Systematic review of 108 studies with a total of 182 patients with interstitial granulomatous dermatitis (IGD). IGD was frequently associated with systemic conditions or drug exposure. Management includes careful medication review and prompt withdrawal of potential triggers. Corticosteroids (systemic and topical) were commonly effective, while biologic
Francesco Bellinato +4 more
wiley +1 more source
OBJECTIVES/SPECIFIC AIMS: Morphea (localized scleroderma) is an autoimmune disease characterized that is widely thought to have a monophasic course, in which an initial period of inflammation (activity) ultimately results in scarring, atrophy, and ...
Stephanie Florez-Pollack +2 more
doaj +1 more source

