Results 61 to 70 of about 7,733 (241)
Morphea masquerading as cellulitis
BMJ Case Reports, 2019 A case of morphea postbreast reconstruction is presented. It is a rare condition that can be easily mistaken for other inflammatory conditions or infection.
Claire Sethu +2 more
openalex +4 more sources
JEADV Clinical Practice, Volume 4, Issue 2, Page 540-543, June 2025.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
Case of generalized morphea complicated with systemic sclerosis
Dermatology Reports, 2021 Dear Editor, Localized scleroderma (LSc; morphea) is a rare fibrosing disease of the skin and underlying tissues, which is different from systemic sclerosis (SSc).
Soichiro Sawamura +4 more
doaj +1 more source
Grundlagen und Wirkprinzipien von wassergefiltertem Infrarot A (wIRA) in Bezug zur Wundheilung [PDF]
, 2006 The experience of the pleasant heat of the sun in moderate climatic zones arises from the filtering of the heat radiation of the sun by water vapor in the atmosphere of the earth.
Hoffmann, Gerd
core +1 more source
Extensive morphea profunda with autoantibodies and benign tumors: A rare case report
Indian Dermatology Online Journal, 2012 The term deep morphea describes a variant of morphea (localised scleroderma) in which inflammation and sclerosis are found in the deep dermis, panniculus, fascia or superficial muscle. It is sometimes associated with autoantibodies. We report the case of
Leelavathy Budamakuntla +1 more
doaj +1 more source
Parry Romberg Syndrome with localized scleroderma: a case report [PDF]
, 2014 Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome
Gupta, Nikita +3 more
core +1 more source
Morphea in Childhood: An Update
Actas Dermo-Sifiliográficas (English Edition), 2018 Morphea is an inflammatory, fibrosing skin disorder. When it occurs in childhood, it is also known as localized juvenile scleroderma. It is more common in girls and typically appears around the age of 5 to 7 years. According to a recent classification system, morphea is divided into 5 types: circumscribed (plaque), linear, generalized, pansclerotic ...
J. Jiménez-Reyes, B. Aranegui
openaire +3 more sources
Severe alopecia complicating systemic sclerosis [PDF]
, 2015 Aims: To describe a case of systemic sclerosis (SSc) associated with severe alopecia areata (AA) responsive to topical and systemic treatments, including vasoactive and immunosuppressive drugs (mycophenolate mofetil). Presentation of the Case: A 56 year
Cassone, Giulia +3 more
core +1 more source
Morphea (Localized Scleroderma) Presenting With Recurrent Skin and Soft Tissue Infections: A Diagnostic Dilemma. [PDF]
, 2020 Morphea or localized scleroderma is reported to be triggered through diverse stimuli. We present a case of morphea that presented as a non-healing wound with superimposed methicillin-sensitive Staphylococcus aureus (MSSA) infection.
Khatri, A. M. +2 more
core +2 more sources
A Guide to Screening for Autoimmune Diseases in Patients With Vulvar Lichen Sclerosus
Australasian Journal of Dermatology, Volume 66, Issue 3, Page 135-141, May 2025.ABSTRACT Background The aetiology of vulvar lichen sclerosus (VLS) remains unknown. However, there is evidence that in addition to a genetic predisposition, autoimmunity contributes to the pathogenesis. Objectives The objective of this study was to determine the prevalence of autoimmune disease and positive autoantibody serology in patients with VLS ...
Annabel Guttentag +5 more
wiley +1 more source