Scleroderma-Like Lupus Panniculitis: A Case Report and Literature Review
Prinpat Pinyowiwat, Suthinee Rutnin, Kumutnart Chanprapaph Division of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, ThailandCorrespondence: Kumutnart Chanprapaph, Division of Dermatology ...
Pinyowiwat P, Rutnin S, Chanprapaph K
doaj
Сучасні аспекти патогенетичної терапії хворих на склеродермію. Огляд літератури [PDF]
Дані літератури свідчать, що традиційні лікарські препарати у хворих на склеродермію ефективні далеко не завжди; багато з них спричиняють різні побічні реакції, що обумовлює пошук принципово нових терапевтичних технологій, у тому числі – з використанням ...
Горбунцов, В.В.+2 more
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Abstract Background Adjuvant immunotherapy (AIO) improved recurrence‐free survival (RFS) in patients with resected stages III–IV melanoma. Real‐world data, especially in elderly patients, as well as optimal management of patients who relpases, are still limited.
Manon Blaise+10 more
wiley +1 more source
A proposed scoring system for assessing the severity of actinic keratosis on the head: actinic keratosis area and severity index [PDF]
Background: Actinic keratosis (AK) severity is currently evaluated by subjective assessment of patients. Objectives: To develop and perform an initial pilot validation of a new easy-to-use quantitative tool for assessing AK severity on the head ...
Arkachaisri+27 more
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Juvenile Localized Scleroderma. Questions of Treatment
Juvenile localized scleroderma (JLS) is a group of childhood diseases with the main symptom — skin and subcutaneous structures lesions, without any organ involvement. There is active (inflammatory) and fibrotic phase in development of JLS.
Rinat K. Raupov, Mikhail M. Kostik
doaj +1 more source
The Interconnected World of Dermatology and Ophthalmology
Medical science, is an integrated field that shares intricate relationship between various organ systems. Similarly, dermatology is inter‐related with various other specialties including ophthalmology. This article depicts the correlation of ophthalmology and dermatology iterating on the genetic diseases, autoimmune diseases, systemic disorders ...
Gyanesh Rathore+4 more
wiley +1 more source
Иммуногистохимический профиль пораженной кожи при системной склеродермии [PDF]
З метою виявлення імуногістохімічних особливостей стану дерми і епідермісу при системній склеродермії було проведено дослідження маркерів: CD3, CD8, CD20, CD79б, CD68, CD1б, CD34, CD105, aSMA, віментин, eNOS, Ki67, колаген IV, bcl2, каспаза 3.
Романенко, К.В.
core
Eosinophilic fasciitis: demographics, disease pattern and response to treatment: report of 12 cases and review of the literature [PDF]
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
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Comorbidities of Primary Scarring Alopecias: A Retrospective Multi‐Site Cross‐Sectional Study
This study was a retrospective chart review evaluating the prevalence of systemic comorbidities in scarring alopecia (n = 240) compared to the general U.S. population. Scarring alopecia patients were found to have higher rates of vitamin D deficiency, metabolic syndrome, depression, anxiety, thyroid disease, uterine fibroids, anemia, atopy ...
Arielle Carolina Mora Hurtado+7 more
wiley +1 more source
Connective Tissue Growth Factor Causes Persistent Proα2(I) Collagen Gene Expression Induced by Transforming Growth Factor-β in a Mouse Fibrosis Model [PDF]
Skin fibrotic disorders such as systemic sclerosis (SSc) are characterized by an excessive production of extracellular matrix (ECM) and understood to develop under the influence of certain growth factors.
Abreu+45 more
core +1 more source