Results 11 to 20 of about 2,887 (195)
Dermoscopy of Lichen Planus Follicularis Tumidus: A Case Report With Pattern Analysis and Literature Review. [PDF]
Clin Case RepABSTRACT Lichen planus follicularis tumidus (LPFT) is a rare variant of lichen planus presenting as erythematous to violaceous plaques with significant follicular involvement, most commonly in the retroauricular area. We report a case demonstrating a novel dermoscopic pattern reminiscent of a follicular galaxy, composed of variably sized comedo‐like ...
Azhari V, Saber M.
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A Rare Case of Coexistence: Discoid Lupus Erythematosus and Sturge-Weber Syndrome. [PDF]
Clin Case RepABSTRACT 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
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Reticular Erythematous Mucinosis: Exclusive Involvement of the Axillary Region
Case Reports in Dermatology, 2021 Reticular erythematous mucinosis is a primary cutaneous mucinosis characterized by the presence of erythematous macules, papules, or plaques coalescing into a reticular pattern that typically involves the midline of the chest or back in middle-aged women.
Martina Burlando +4 more
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Case Reports in Dermatology, 2023 Reticular erythematous mucinosis is a rare and persistent form of primary idiopathic mucinosis, often referred to as plaque-like cutaneous mucinosis or midline mucinosis.
Daniela Tenea, Cinzia Campaini
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SAGE Open Medical Case Reports, 2021 Reticular erythematous mucinosis is an uncommon type of cutaneous mucinosis. Typically, reticular erythematous mucinosis affects middle-aged women and usually appears as papules and plaques on the mid-upper trunk.
Bret Kenny +3 more
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Cutaneous mucinosis in mixed connective tissue disease* [PDF]
Anais Brasileiros de Dermatologia, 2013 Cutaneous mucinosis is a group of conditions involving an accumulation of mucin or glycosaminoglycan in the skin and its annexes. It is described in some connective tissue diseases but never in association with mixed connective tissue disease.
Maria Helena Sampaio Favarato +5 more
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Cutaneous mucinosis of infancy: a rare case of joint involvement
Pediatric Rheumatology Online Journal, 2021 Background Primary cutaneous mucinosis are a heterogeneous group of diseases characterized by the deposition of glycosaminoglycans in the dermis and the follicles.
Cristina Morreale +3 more
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Follicular mucinosis: an important differential diagnosis of leprosy in an endemic area [PDF]
Anais Brasileiros de Dermatologia, 2015 Primary follicular mucinosis is a rare dermatosis characterized by the accumulation of mucin in the follicular epithelium and sebaceous glands. Clinically, it is characterized by the presence of papules or well-circumscribed and infiltrated plaques.
Danielle Cristine Westphal +5 more
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Skin-Colored Papules on the Face and Chest of a Female Patient. [PDF]
Clin Case RepABSTRACT 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