Results 71 to 80 of about 7,562 (197)

Immunohistochemical Similarities between Lichen Sclerosus et Atrophicus and Morphea: A Case Study

open access: yesCase Reports in Dermatology, 2015
Both morphea and lichen sclerosus et atrophicus (LSA) are connective tissue diseases that mainly affect the skin. A recent report suggested that a substantial portion of morphea coexists with LSA.
Aya Kakizaki   +4 more
doaj   +1 more source

Development of keloidal morphea after treatment with cyclosporine in a case of recalcitrant generalized morphea

open access: yesClinical Case Reports, 2020
Nodular or keloidal morphea, also known as nodular scleroderma, is a rare form of localized sclerosis (SSc) or morphea. In this paper, we reported a case of this rare entity with a review of the literature.
Sahar Dadkhahfar   +3 more
doaj   +1 more source

Morphea on the Breast after a Needle Biopsy [PDF]

open access: yes, 2011
Localized scleroderma (morphea) usually develops spontaneously, but the precise mechanisms underlying disease development are obscure. However, a significant number of cases suggest that morphea is induced by external stimuli. Herein, we report a case of
Arase, Noriko   +5 more
core   +2 more sources

LC‐OCT for early diagnosis and characterization of dermatologic adverse events to oncologic drugs and correlation to histopathology

open access: yesInternational Journal of Dermatology, Volume 64, Issue 4, Page 719-724, April 2025.
Abstract Background Targeted and immune therapies have recently been associated with the occurrence of multiple cutaneous toxicities, often challenging to differentiate by clinical examination alone without histology. Line‐field confocal optical coherence tomography (LC‐OCT) is a non‐invasive and innovative imaging technique that has been shown to be ...
Pietro Sollena   +9 more
wiley   +1 more source

Navigating into the Dental Management of a Child with Morphea: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Morphea, a morphological variant of Localised Scleroderma (LoS) that typically occurs in children, is an inflammatory disease of connective tissue leading to skin and underlying tissue sclerosis due to increased deposition of collagen.
Shrayana Bhattacharya   +3 more
doaj   +1 more source

Histopathology of morphea: Sensitivity of various named signs, a retrospective study

open access: yesIndian Journal of Pathology and Microbiology, 2020
Background: Morphea or localized scleroderma is characterized histopathologically by sclerosis, fibrosis, and atrophy of the skin and subcutaneous tissue.
Rashmi Jindal   +2 more
doaj   +1 more source

Multiple Mucous Cysts on the Hands of a Patient With Systemic Sclerosis Treated With Collagen Sheets for Scar Healing

open access: yes
The Journal of Dermatology, Volume 52, Issue 6, Page e529-e530, June 2025.
Takano Hobo   +6 more
wiley   +1 more source

Early morphea simulating patch-stage mycosis fungoides in two cases

open access: yesDermatology Reports, 2018
Morphea is a skin disorder characterized by thickening of dermis and subcutaneous tissues and loss of adnexal structures. In the early inflammatory stage of morphea, diagnostic histological findings are absent and this may lead to confusion with other ...
Hamid R. Ghasemi Basir   +3 more
doaj   +1 more source

Lokalisierte Sklerodermie (Morphea) im Kindesalter [PDF]

open access: yes, 2018
Zusammenfassung: Die lokalisierte (oder zirkumskripte) Sklerodermie (LS) oder Morphea ist eine sklerosierende Bindegewebserkrankung der Haut, die auch darunterliegende Gewebe wie Subkutis, Muskulatur und Skelett betreffen kann.
Weibel, L.
core  

Eosinophilic fasciitis: demographics, disease pattern and response to treatment: report of 12 cases and review of the literature [PDF]

open access: yes, 2007
BACKGROUND: Eosinophilic fasciitis is a rare scleroderma-like illness. The clinical spectrum of the disease has evolved since its initial description. METHODS: We identified all patients diagnosed with eosinophilic fasciitis over the past 10 years at our
Bischoff, Lindsay, Derk, Chris T
core   +2 more sources

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