Results 11 to 20 of about 1,378 (169)
Dermoscopy of Lichen Planus Follicularis Tumidus: A Case Report With Pattern Analysis and Literature Review. [PDF]
ABSTRACT 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.
europepmc +2 more sources
Scleromyxedema Managed With High-Dose Intravenous Immunoglobulin and Bortezomib-Dexamethasone: A Case Report. [PDF]
Scleromyxedema is a rare, chronic cutaneous mucinosis marked by widespread waxy papules and potential extracutaneous involvement. This case report discusses the management of a 48‐year‐old female diagnosed with scleromyxedema, who initially partially responded to high‐dose intravenous immunoglobulin (HDIVIG) therapy.
Wijaya D, Hanson Z, Lau EK, Akhtari M.
europepmc +2 more sources
Recurrent Cutaneous Myxoma of the Eyelid: A Case Report. [PDF]
Cutaneous myxomas are rare, benign mesenchymal tumors of the dermis. They may occur in isolation or as part of genetic syndromes and can affect the head and neck regions, yet eyelid involvement is rare. We report a case of a 24‐year‐old male with a 10‐year history of a recurrent right upper eyelid lesion, previously excised five times.
Fonseca MI +3 more
europepmc +2 more sources
A Rare Case of Coexistence: Discoid Lupus Erythematosus and Sturge-Weber Syndrome. [PDF]
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
Cutaneous mucinosis in mixed connective tissue disease* [PDF]
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
doaj +1 more source
Cutaneous mucinosis of infancy: a rare case of joint involvement
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
doaj +1 more source
Follicular mucinosis: an important differential diagnosis of leprosy in an endemic area [PDF]
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
doaj +1 more source
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
Case of follicular mucinosis showing brownish yellow and red dots via dermoscopy
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

