Results 41 to 50 of about 1,472 (169)
Treatment of scleromyxedema Arndt-Gottron with a novel intravenous immunoglobulin preparation
Dermatology ReportsDear Editor, Scleromyxedema is known as a rare, severe mucinosis with characteristic waxy skin papules along with sclerodermiform induration of the skin and rare systemic manifestations. Monoclonal gammopathy of undetermined significance (MGUS; mostly
Niklas Negele +2 more
doaj +1 more source
Acta Medica Iranica, 1996 Scleromyxedema is a rare, chronic, progressive, fibromucinous disorder of unknown etiology, characterized by lichenoid waxy papules and firm induration of skin of trunk, face, forearm and hands; fibroblast proliferation and mucin deposition in the upper ...
Z. Safaii Naraghi. +1 more
doaj +2 more sources
Topical Imiquimod in Mycosis Fungoides: A Systematic Review of Published Clinical Evidence
Dermatologic Therapy, Volume 2026, Issue 1, 2026.Background Topical imiquimod has been used as a skin‐directed treatment in selected patients with mycosis fungoides, but the available evidence remains limited and scattered across case reports, case series, pilot studies, retrospective cohorts, and preliminary conference data.
Kerem Balan +2 more
wiley +1 more source
Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
Dermatologic Therapy, Volume 2026, Issue 1, 2026.Folliculotropic mycosis fungoides (FMF) is a rare subtype of MF, characterized by prominent folliculotropism in histopathology. Clinically, FMF exhibits polymorphic presentations, mainly including follicular papules, plaques, alopecia, and other nonspecific lesions, with a predilection for the head and neck region, leading to frequent misdiagnosis ...
Xingyu Li, Jie Liu, Nicola Pimpinelli
wiley +1 more source
Clinical Case Reports, 2023 Key Clinical Message In reticular erythematous mucinosis, (1) the presence of dotted vessels and (2) uniform, structureless, yellowish‐white spots, and patches on dermoscopy correspond to histopathological findings of (1) vessels at the tips of the ...
Tomoaki Takada
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Dermatologic Therapy, Volume 2026, Issue 1, 2026.Background The clinical characteristics of hydroxychloroquine (HCQ)‐induced acute generalized exanthematous pustulosis (AGEP) remain inadequately defined. This research sought to define the incidence and clinical course of AGEP following HCQ administration.
Fei Lu +3 more
wiley +1 more source
Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2004 Desde 1957 se han descrito pacientes con alopecia localizada, caracterizada en la histopatología por el depósito de mucina dentro.de los folículos pilosos (mucinosis folicular).
Gerardo Arellano Sánchez +5 more
doaj
Alopecia mucinosa responding to antileprosy treatment: Are we missing something?
Indian Journal of Dermatology, 2013 Three cases with single lesion of Alopecia mucinosa (follicular mucinosis) were treated with antileprosy treatment and showed rapid and complete resolution of the lesions with no recurrence on extended follow-up.
Rajiv Joshi, Vinay Gopalani
doaj +1 more source
Hyalase in Dermatology: Applications Beyond Filler Management
Journal of Cosmetic Dermatology, Volume 24, Issue 11, November 2025.ABSTRACT Background Hyaluronic acid (HA) is a key extracellular matrix component in the skin. Hyaluronidase is an enzyme that breaks down HA into monosaccharides. The FDA has approved this enzyme for hypodermoclysis, drug absorption enhancement, and subcutaneous urography.
Saba Hasanzadeh +6 more
wiley +1 more source
A Rare Clinical Presentation of Congenital Superficial Angiomyxoma: A Case Report
Clinical Case Reports, Volume 13, Issue 10, October 2025.A pedunculated, cauliflower red‐colored, jelly mass in the left vulvar region (A) & (B). ABSTRACT Angiomyxoma is a rare atypical mesenchymal proliferation with two distinct forms, deep and superficial. Superficial Angiomyxoma tends to be benign with limited skin involvement.
Saman Al‐Zahawi +6 more
wiley +1 more source