Results 41 to 50 of about 1,378 (169)

Clinical Characteristics, Treatment, and Prognosis of Hydroxychloroquine‐Induced Acute Generalized Exanthematous Pustulosis

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, Ying Song, Chunjiang Wang, Suraiya Saleem   +3 more
wiley   +1 more source

Acral papular mucinosis: a new case of this rare entity [PDF]

Anais Brasileiros de Dermatologia, 2016
Acral persistent papular mucinosis (APPM) is a rare subtype of localized lichen myxedematosus. It consists of small papules localized exclusively on the back of the hands, wrists and extensor aspects of distal forearms with no other clinical or ...
María Encarnación Gómez Sánchez, Fernando de Manueles Marcos, Maria Luisa Martínez Martínez, Roberto Vera Berón, Jose Manuel Azaña Défez   +4 more
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, Parisa Farokh, Golsa Sadat Hosseini, Maryam Abbasian, Ifa Etesami, Shirin Zaresharifi, Sahar Dadkhahfar   +6 more
wiley   +1 more source

SCLEROMYXEDEMA [PDF]

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., P. Mansouri M.R. Mortazavi   +1 more
doaj   +2 more sources

Sclerosing diseases of the skin

JDDG: 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, Katharina Meier, Kamran Ghoreschi, Maria Kinberger, Farzan Solimani   +4 more
wiley   +1 more source

Reticular erythematous mucinosis: Relationship between its dermoscopic and histopathological findings

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
doaj   +1 more source

Successful Multimodal Therapeutic Approach for CD30‐positive Folliculotropic Mycosis Fungoides

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Chiara L. Blomen, Inga Hansen‐Abeck, Andrea Baehr, Stefan W. Schneider, Christoffer Gebhardt, Nina Booken   +5 more
wiley   +1 more source

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

Clinical 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, Jingjing Zeng, Peiying Zhong, Chengyao Jia, Li Zhang   +4 more
wiley   +1 more source

Epidermal Nevi and Epidermal Naevus Syndromes

JEADV 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, Beatrice Carcano, Michela Brena   +2 more
wiley   +1 more source

Oral focal mucinosis in a dog with brachycephalic obstructive airway syndrome

Veterinary Record Case Reports, Volume 13, Issue 2, June 2025.
Abstract Oral focal mucinosis is an uncommon disorder primarily reported in people and characterised by excessive hyaluronic acid production in the mucosa. This report describes a novel occurrence of oral focal mucinosis in a 3‐year‐old French Mastiff with brachycephalic obstructive airway syndrome, presenting with severe respiratory distress and mucin
Daiana R. Cardoso, João Martins, Ana Resendes, Sónia Campos   +3 more
wiley   +1 more source