Results 61 to 70 of about 792 (148)

Successful Treatment of Hemifacial Myokymia and Dystonia Associated to Linear Scleroderma “En Coup de Sabre” with Repeated Botox Injections

open access: yesCase Reports in Medicine, 2012
Linear scleroderma “en coup de sabre” (LSCS) is a form of localized scleroderma presents as band-like sclerotic lesions of the frontoparietal area. It has been reported in association with diverse neurological manifestations like seizures, migraine ...
Carlos A. Cañas   +3 more
doaj   +1 more source

A Surgical Approach for Stable Lesions of Linear Scleroderma

open access: yesKaohsiung Journal of Medical Sciences, 2010
A 29-year-old Japanese woman presented with alopecia lesions in her occipital region and was diagnosed as linear scleroderma. Topical steroids along with psoralen and UVA light therapy were applied, but the lesion persisted.
Hiroshi Kato   +3 more
doaj   +1 more source

S2k guideline: Diagnosis and therapy of localized scleroderma

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.
Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter   +12 more
wiley   +1 more source

Generalized morphea following radiotherapy for an intracranial tumor

open access: yesIndian Journal of Dermatology, 2016
Morphea is a localized scleroderma variety which can be circumscribed or generalized and is characterized by sclerotic plaques developing on trunk and limbs. Surgery and radiation have been implicated as etiological factors for the development of morphea.
Shrenik Balegar   +4 more
doaj   +1 more source

High‐Frequency Ultrasound Assessment of Skin Thickness Following Lipofilling in Facial Sclerosing Dermatoses: A Case Series

open access: yes
Journal of Cosmetic Dermatology, Volume 24, Issue 5, May 2025.
Sofia Gomez‐Martinez   +12 more
wiley   +1 more source

S2k‐Leitlinie: Diagnostik und Therapie der zirkumskripten Sklerodermie

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-621, April 2024.
Zusammenfassung Die vorliegende aktualisierte S2k‐Leitlinie befasst sich mit der Diagnostik und der Therapie der zirkumskripten Sklerodermie (ZS). Diese umfasst ein Spektrum sklerotischer Erkrankungen der Haut mit, je nach Subtyp und Lokalisation, möglicher Beteiligung von hautnahen Strukturen wie Fettgewebe, Muskulatur, Gelenke und Knochen. Ein Befall
Alexander Kreuter   +12 more
wiley   +1 more source

Systematic Review of Health‐Related Quality of Life Impact in Juvenile Localized Scleroderma

open access: yesArthritis Care &Research, Volume 76, Issue 3, Page 340-349, March 2024.
Objective The prevalence and types of psychosocial complications of juvenile localized scleroderma (JLS), also known as morphea, an inflammatory and sclerosing disease involving the skin, fascia, muscle, and bone, are poorly understood. Methods We performed a systematic review of literature published between 2000 and 2020 in PubMed, EMBASE, the ...
Luis F. Sanchez‐Espino   +5 more
wiley   +1 more source

Ipsilateral Coat′s reaction in the eye of a child withen coup de sabre morphoea-A case report

open access: yesIndian Journal of Ophthalmology, 1992
A female child with post-traumatic en coup de sabre type of morphoea (fronto-parietal circumscribed scleroderma) involving the left side of the forehead and face, who developed a Coat′s disease-like fundus picture over the following two years, is ...
Neki A, Sharma A
doaj  

Clinical Characteristics and Prognosis of Morphea (Localized Scleroderma) in Adults: a Retrospective Study

open access: yesSiriraj Medical Journal, 2019
Objective: To study the clinical characteristics and prognosis of morphea in Thai adult patients.  Methods: The medical records of 81 morphea adult patients who visited Siriraj Hospital, Thailand, between 2006 and 2015, were retrospectively reviewed. The
Narumol Silpa-archa   +3 more
doaj   +3 more sources

Idiopathic acquired progressive left facial hemiatrophy (Parry-Romberg syndrome) in a 21-year-old man in semi-urban, south-west Nigeria

open access: yesSouth African Family Practice, 2011
Idiopathic progressive hemifacial atrophy, or Parry-Romberg syndrome, is a rare entity, seldom described in medical texts. Though first described in 1825, as yet there are no clear-cut diagnostic criteria. It is of interest mainly because of the numerous
F.A. Imarhiagbe, A.O. Adeoti
doaj   +1 more source

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