Results 21 to 30 of about 1,420 (166)

Case of follicular mucinosis showing brownish yellow and red dots via dermoscopy

open access: yesClinical Case Reports, 2022
We herein describe a 68‐year‐old man with follicular mucinosis. A dermoscopic examination showed multiple, round, brownish yellow dots with a whitish rim in the follicular ostium and red dots in the interfollicular area.
Hiroki Yamagishi   +3 more
doaj   +1 more source

Case report: Sublingual mucinosis in a dog

open access: yesFrontiers in Veterinary Science, 2022
A 11-month-old male intact Shar-Pei (26. 5 kg) was presented for a bilateral sublingual swelling of 4 months duration. The exploration of the oral cavity highlighted the presence of bilateral sublingual swellings, primarily consistent with bilateral ...
Debora Tinto   +4 more
doaj   +1 more source

A Rare Case of Coexistence: Discoid Lupus Erythematosus and Sturge-Weber Syndrome. [PDF]

open access: yesClin Case Rep
ABSTRACT This rare coexistence of Sturge–Weber Syndrome (SWS) and discoid lupus erythematosus (DLE) presents unique diagnostic and therapeutic challenges. It highlights potential shared environmental triggers and overlapping inflammatory mechanisms, underscoring the need for a multidisciplinary approach to management.
Efazati A   +4 more
europepmc   +2 more sources

Mucinosis papular

open access: yesRevista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2006
La mucinosis papular o liquen mixedematoso localizado se caracteriza por la presencia de pápulas, nódulos o placas liquenoides debidos al depósito dérmico de mucina y a fibrosis variable.
Fabián Andrés Hernández Velasco   +1 more
doaj   +1 more source

Severe cutaneous scleromyxedema treated by lenalidomide

open access: yesJEADV Clinical Practice, 2023
Scleromyxedema is a rare clinical variant of primary cutaneous mucinosis. It is defined by a generalized papular and sclerodermoid eruption associated with monoclonal gammopathy. No specific definitive treatment is known and those tried have inconsistent
Théo Brochet   +9 more
doaj   +1 more source

Oral focal mucinosis of palatal mucosa: A rare case report

open access: yesContemporary Clinical Dentistry, 2012
Oral focal mucinosis (OFM), an oral counterpart of cutaneous focal mucinosis, is a rare disease of unknown etiology. Its pathogenesis may be due to the overproduction of hyaluronic acid by a fibroblast, at the expense of collagen production, resulting in
Bharti Vipin, Singh Jagmohan
doaj   +1 more source

Primary follicular mucinosis – case report

open access: yesMedicina, 2017
Of unknown etiology, acute follicular mucinosis is clinically characterized as an inflammatory disease coursing with more or less infiltrated and scaly plaques, with or without hair loss.
Laura Loures Tavares   +4 more
doaj   +1 more source

Diagnosis and treatment of oral focal mucinosis: a case series

open access: yesJournal of Medical Case Reports, 2019
Background Oral focal mucinosis, the oral counterpart of cutaneous focal mucinosis, is a rare disease. As it has no characteristic clinical or radiological features, diagnosis is established by histopathological and immunohistological examination.
Yusuke Higuchi   +6 more
doaj   +1 more source

Cutaneous mucinosis of infancy

open access: yesJAAD Case Reports, 2016
We present a case of a 4-year-old fair-skinned girl, with no significant medical history, who presented to the outpatient clinic of an academic medical center with an asymptomatic, flesh-colored, cobblestoned plaque on her lateral left thigh (Fig 1).
Reddy, Swapna C.   +3 more
openaire   +2 more sources

Skin-Colored Papules on the Face and Chest of a Female Patient. [PDF]

open access: yesClin Case Rep
ABSTRACT Scleromyxedema is an unpredictable but progressive disease and can be lethal due to systemic involvement if not diagnosed timely. Hence, we require a keen observational clinical eye to diagnose the condition from its differentials, along with further research into treatment modalities to treat this condition.
Ghahartars M   +3 more
europepmc   +2 more sources

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