Results 71 to 80 of about 1,291 (187)

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

Sclerosing diseases of the skin

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1301, October 2025.
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari   +4 more
wiley   +1 more source

Skin‐Colored Papules on the Face and Chest of a Female Patient

open access: yesClinical Case Reports, Volume 13, Issue 9, September 2025.
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.
Mehdi Ghahartars   +3 more
wiley   +1 more source

Cutaneous mucinosis associated with multiple frozen joints and bony heterotopic deposits around the hips.

open access: yes, 1986
A 43-year-old man suffered from migrating then additive arthralgias associated with macroscopic and microscopic cutaneous lesions compatible at first sight with reticular erythematous mucinosis.
Maldague, Baudouin   +5 more
core   +1 more source

Monoclonal Gammopathies of Clinical Significance—Scleromyxedema: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Scleromyxedema is an uncommon, chronic connective tissue disorder with an obscure etiology. It is distinguished by fibromyxoid skin lesions and elevated serum monoclonal immunoglobulin levels. The condition's rarity limits epidemiological data, making prevalence and incidence assessment difficult.
Shanshan Liang   +4 more
wiley   +1 more source

Cutaneous mucinosis in shar-pei - Case report

open access: yes, 2020
Cutaneous mucinosis is the excessive deposition of mucin in the dermis and hair follicles, being frequent in Shar-Pei dogs due to their skin roughness.
Pinheiro, Breno Queiroz   +4 more
core  

Monoclonal gammopathy of undetermined significance-associated scleromyxoedema

open access: yesIndian Dermatology Online Journal, 2019
Scleromyxoedema is a rare generalized cutaneous mucinosis, which in absence of thyroid disease, occurs almost invariably in patients with monoclonal gammopathies.
Kalgi D Baxi   +3 more
doaj   +1 more source

Epidermal Nevi and Epidermal Naevus Syndromes

open access: yesJEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.
ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini   +2 more
wiley   +1 more source

Self-Healing Juvenile Cutaneous Mucinosis: A Report of Two Cases With Differing Evolution.

open access: yes, 2023
20.500.12530/87909Self-healing juvenile cutaneous mucinosis is a rare entity, characterized by the presence of subcutaneous nodules together with frequent nonspecific systemic symptoms, which occurs in the pediatric age and characteristically resolves ...
Reneses-Prieto, Elvira   +9 more
core   +1 more source

A Case of Cutaneous Focal Mucinosis with Onychomycosis

open access: yes, 2018
Cutaneous focal mucinosis was first described by Johnson and Helwig in 1961 and is histologically characterized by localized accumulation of mucin in the upper and middermis with scattered spindle-shaped fibroblasts.
명기범, 최혜영
core  

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