Results 131 to 140 of about 7,212 (260)

Survival among patients with systemic sclerosis‐associated pulmonary arterial hypertension in the Australian scleroderma cohort study

open access: yesInternal Medicine Journal, EarlyView.
Abstract Background and Aims Systemic sclerosis (scleroderma; SSc) patients can develop pulmonary arterial hypertension (PAH), which is a leading cause of death. We sought to evaluate severity, therapeutic strategy and survival of SSc‐PAH in the Australian Scleroderma Cohort Study (ASCS).
Zoe Brown   +13 more
wiley   +1 more source

Male genital lichen sclerosus

open access: yesJournal of the European Academy of Dermatology and Venereology, EarlyView.
Male genital lichen sclerosus is driven by chronic, occluded exposure of susceptible genital epithelium to urine, rather than infection or autoimmunity. This review synthesizes clinical, anatomical and molecular evidence showing how microincontinence and occlusion initiate inflammation, fibrosis and carcinogenesis, and explains the curative effect of ...
Georgios Kravvas   +3 more
wiley   +1 more source

Basal cell carcinoma in dark skin: clinical and dermoscopy features. [PDF]

open access: yesAn Bras Dermatol
Valadares PJC   +3 more
europepmc   +1 more source

Restoring Mouth Opening in Systemic Sclerosis: A Scoping Review of Interventions

open access: yesOral Diseases, EarlyView.
ABSTRACT Objectives To map and characterize the therapeutic strategies described in the literature for the management of microstomia in patients with systemic sclerosis. Methods This scoping review was conducted in accordance with the PRISMA‐ScR guidelines. Searches were performed in Medline/PubMed, Embase, Scopus, Web of Science, Cochrane Library, and
Beatriz Borba Barros Bernardo   +5 more
wiley   +1 more source

Cutaneous Rosai-Dorfman-Destombes disease: the diagnostic value of the yellow island sign. [PDF]

open access: yesOxf Med Case Reports
El Maati M   +4 more
europepmc   +1 more source

Nail Clubbing‐Associated With a Large Segmental Infantile Hemangioma of the Arm in a Patient With PHACES Syndrome

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Although infantile hemangiomas (IH) are common vascular tumors of childhood, associated nail abnormalities are rare. We report a child with a large segmental IH of the upper limb with marked, ipsilateral nail clubbing, which gradually improved until the age of 7 years.
Stefan Blunder   +5 more
wiley   +1 more source

Plaque‐type trichoblastoma and its siblings: A (follicular tumour) family history

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Ines Bertlich   +4 more
wiley   +1 more source

Solitary Lesion With Features of Atrophic Papulosis in Early Childhood

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Atrophic papulosis (Köhlmeier‐Degos disease) is a rare thrombo‐occlusive vasculopathy classically presenting with multiple porcelain‐white atrophic papules and a high risk of progression to systemic involvement. We report a 2‐year‐old girl presenting with clinical, dermoscopic, and histologic findings of atrophic papulosis with only a solitary
Ou Jia Emilie Wang   +4 more
wiley   +1 more source

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