Results 71 to 80 of about 4,842 (201)
Therapeutic advances in the treatment of vasculitis [PDF]
Considerable therapeutic advances for the treatment of vasculitis of the young have been made in the past 10 years, including the development of outcome measures that facilitate clinical trial design.
Brogan, PA, Eleftheriou, D
core +2 more sources
Mycoplasma pneumoniae‐Associated Mucositis: A Diagnostic Dilemma
ABSTRACT Fuchs syndrome is a mucosal variant of Stevens‐Johnson syndrome (SJS) without cutaneous lesions, mostly affecting the mucosa of the mouth, conjunctiva, and genitalia, that occurs in a background of Mycoplasma pneumoniae and herpes simplex infection. Treatment with antibiotics such as macrolides, tetracycline, or fluoroquinolones has been shown
Mahesh Mathur +5 more
wiley +1 more source
2015 Annual Meeting of the Medical Dermatology Society [PDF]
Von J ...
Jettinger, J.
core +1 more source
Journal of Hospital Medicine, Volume 21, Issue 2, Page 200-204, February 2026.
Gurpreet Dhaliwal +4 more
wiley +1 more source
Efficacy and Safety of Topical Dapsone in Dermatology: A Scoping Review of Clinical Studies
ABSTRACT Background Dapsone (4,4′‐Diamino diphenyl sulfone) has been utilized in managing a wide variety of mucocutaneous conditions, usually as a systemic product. Topical dapsone is commercially available as 5% and 7.5% gel and is FDA‐approved for acne vulgaris.
Bahareh Abtahi‐Naeini +4 more
wiley +1 more source
IgA Vasculitis Across the Ages: Is It Time for a Precision Medicine Approach?
IgA vasculitis (IgAV; formerly Henoch‐Schönlein purpura) is a systemic small vessel vasculitis most commonly affecting the skin, gut, joints, and kidneys. Nephritis is the most concerning complication for all ages because it carries the risk of progression to irreversible end‐stage kidney failure.
A. Gage +4 more
wiley +1 more source
Oxacillin-induced leukocytoclastic vasculitis
Leukocytoclastic vasculitis (LCV) refers to a histopathological pattern of neutrophil predominant inflammatory process of small vessels associated with fibrinoid necrosis.
Meric Mericliler +4 more
doaj +1 more source
Interstitial granulomatous dermatitis due to borreliosis [PDF]
3Interstitial granulomatous dermatitis (IGD) is a rare dermatosis of unknown cause with characteristic histopathological features and variable clinical expression.
Di Meo, Nicola +2 more
core +3 more sources
Impending Central Retinal Vein Occlusion in Patient With Idiopathic Cutaneous Leukocytoclastic Vasculitis [PDF]
Purpose: To report a case of impending central retinal vein occlusion (CRVO) associated with idiopathic cutaneous leukocytoclastic vasculitis (LCV) that demonstrated significant resolution following treatment with intravenous (IV) methylprednisolone ...
Akhavanrezayat, Amir +9 more
core +2 more sources
Double ANCA‐negative Granulomatosis with polyangiitis in an Ethiopian man: a diagnostic challenge highlighting the need for clinicopathologic correlation. ABSTRACT This case highlights the importance of considering ANCA‐negative granulomatosis with polyangiitis (GPA) in patients with nonspecific symptoms with multisystem involvement, including ...
Alazar Sitotaw +13 more
wiley +1 more source

