Drug‐Induced Fuchs Syndrome With Isolated Oral Involvement: A Rare Case Report
Stevens–Johnson syndrome (SJS) is a rare, potentially life‐threatening mucocutaneous disorder characterized by epidermal necrosis and mucosal bullous lesions involving less than 10% of the total body surface area. The majority of cases are aggravated by delayed hypersensitivity reactions to medications.
Salina Paudel +6 more
wiley +1 more source
Toxic epidermal necrolysis-like subacute cutaneous lupus erythematosus following pembrolizumab therapy. [PDF]
Marchionni E +4 more
europepmc +1 more source
AB0569 THE EFFECT OF CUTANEOUS AND MUSCULOSKELETAL SYMPTOMS ON QUALITY OF LIFE IN PATIENT WITH SYSTEMIC LUPUS ERYTHEMATOSUS IN RENAISSANCE COHORT [PDF]
L. Vorobyova +2 more
openalex +1 more source
Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
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
Orchestration of Skin Pathology in Cutaneous Lupus Erythematosus by HLA Class I Down-Regulated Senescent Epidermal Basal Cells. [PDF]
Yamamoto S +13 more
europepmc +1 more source
Positive Direct Immunofluorescence in Rowell Syndrome: Further Support for a Subtype of Cutaneous Lupus Erythematosus. [PDF]
Bissenas A +3 more
europepmc +1 more source
Recognition of PPI-Induced Subacute Cutaneous Lupus Erythematosus in Clinical Practice
American Medical Association 2025 +1 more
openalex +1 more source

