Results 41 to 50 of about 37,892 (190)
Cephalexin-Induced Leukocytoclastic Vasculitis
Cureus, 2022 Although allergies to antibiotics are commonly stated, allergies to cephalosporin antibiotics are uncommonly reported. Furthermore, dermatologic and systemic reactions from cephalosporin exposure involving end-organ damage are rare. We present a case of cephalexin, a cephalosporin, induced hypersensitivity vasculitis causing characteristic non ...
Tang, Wesley, Tan, Jennie
openaire +2 more sources
Toxic Shock Syndrome Toxin-1-producing Staphylococcus aureus Bacteremia and Exanthematous and Purpuric Disease with Leukocytoclastic Vasculitis in an Infant [PDF]
, 2018 Staphylococcus aureus exotoxin toxic shock syndrome toxin-1 (TSST-1) can cause a wide spectrum of immunopathological conditions, from toxic shock syndrome (TSS), a life-threatening illness, to neonatal TSS-like exanthematous disease (NTED), a self ...
Shirakawa, Toshihiko +7 more
core
JEADV Clinical Practice, EarlyView.ABSTRACT Sweet's syndrome is a rare neutrophilic dermatosis characterized by an acute onset of erythematous and infiltrative lesions. Diagnosis is based on clinical, histopathological, and laboratory findings. We propose that non‐invasive skin imaging techniques, such as line‐field confocal optical coherence tomography (LC‐OCT), may be beneficial for ...
Aleksandra Anderson +5 more
wiley +1 more source
A case of glyburide-induced leukocytoclastic vasculitis [PDF]
, 2013 Introduction: Medication-induced leukocytoclastic vasculitis is a small-vessel vasculitis that most commonly manifests with palpable purpuric lesions on gravity dependent areas.
Fraga, Garth R +4 more
core +1 more source
Revista do Instituto de Medicina Tropical de São Paulo, 2020 Dengue is a viral disease, caused by an arbovirus of the genus Flavivirus. In Brazil, its incidence rate is high with a broad clinical spectrum. This report discusses a rare case of dengue associated with cutaneous leukocytoclastic vasculitis and ...
Laurisson Albuquerque da Costa +5 more
doaj +1 more source
Allergy, EarlyView.This study aimed to assess diagnostic delay among patients with eosinophilic granulomatosis with polyangiitis (EGPA) and identify clinical characteristics associated with delayed recognition. EGPA diagnosis was delayed by nearly five years from symptom onset in this single‐center cohort.
Vani Mulkareddy +9 more
wiley +1 more source
A Case Report of Leukocytoclastic Vasculitis: Diagnostic Approach and Treatment
, 2023 Patient: Female, 37-year-old Final Diagnosis: Leukocytoclastic vasculitis Symptoms: Severe rash Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Unusual clinical course BACKGROUND: Leukocytoclastic vasculitis is a small-vessel vasculitis associated
Strubchevska, Kateryna +3 more
core +1 more source
Case Reports in Gastrointestinal Medicine, 2021 Ulcerative colitis is an inflammatory bowel disease that in rare cases may develop extraintestinal manifestations. This case report aims to add to the limited clinical data on leukocytoclastic vasculitis and possible ANCA-associated vasculitis as rare ...
Jacky Ng +2 more
doaj +1 more source
Dermatologic Diagnosis: Leukocytoclastic Vasculitis [PDF]
The Permanente Journal, 2015 Leukocytoclastic vasculitis (LCV), also termed hypersensitivity vasculitis, is a small-vessel vasculitis. The skin is the organ most commonly involved in LCV. Typical presentation is a painful, burning rash predominantly in the lower extremities. The most common skin manifestation is palpable purpura.
Joseph, Einhorn, Joel T, Levis
openaire +2 more sources
A case of leukocytoclastic vasculitis caused by novel anticoagulant rivaroxaban [PDF]
, 2017 Cutaneous leukocytoclastic vasculitis (LCV) is type of small vessel vasculitis that commonly presents as palpable purpura involving the lower extremities and buttocks.
Jahan-Tigh, Richard +3 more
core +1 more source