Results 31 to 40 of about 4,842 (201)

Oxaliplatin-Induced Leukocytoclastic Vasculitis under Adjuvant Chemotherapy for Colorectal Cancer: Two Cases of a Rare Adverse Event [PDF]

open access: yes, 2013
Leukocytoclastic vasculitis is a multicausal systemic inflammatory disease of the small vessels, histologically characterized by inflammation and deposition of both nuclear debris and fibrin in dermal postcapillary venules. The clinical picture typically
Conradi, Lena-Christin   +13 more
core   +2 more sources

Koebner phenomenon in leukocytoclastic vasculitis: A case report and an updated review of the literature

open access: yesSAGE Open Medical Case Reports, 2019
Leukocytoclastic vasculitis is the most common form of cutaneous vasculitis. It is a neutrophilic small vessel vasculitis resulting from the deposition of circulating immune complexes.
Farah Kassam   +2 more
doaj   +1 more source

Clinicopathological Features of Cutaneous Vasculitis: A Cross-sectional Study from a Tertiary Care Centre in Karnataka, India [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2023
Introduction: Cutaneous vasculitis is an inflammatory disease of the dermal blood vessels with varying clinical presentations. It is not a single disease but a spectrum of entities that present as cutaneous vasculitis. Hence, histopathological evaluation
Kanthilatha Pai   +3 more
doaj   +1 more source

Acute hemorrhagic edema of infancy (AHEI): Alarming cutaneous presentation of a benign and self‐limited disease

open access: yesClinical Case Reports, 2022
Acute hemorrhagic edema of infancy (AHEI) is a cutaneous leukocytoclastic vasculitis. We report on an 11‐month‐old boy, presenting the classical feature of AHEI with alarming cutaneous presentation, but good clinical condition.
Mario Tumminello   +8 more
doaj   +1 more source

DRESS: características clinicopatológicas em 10 casos de Hospital Universitário em São Paulo [PDF]

open access: yes, 2012
BACKGROUND: Drug reaction with eosinophilia and systemic symptoms is a severe form of drug-induced reaction with multiorgan involvement. OBJECTIVES: The aim of this study is to evaluate the epidemiological, clinical and pathological features and ...
Botelho, Luciane Francisca Fernandes   +4 more
core   +4 more sources

Alcohol-Associated Immunoglobulin A Vasculitis: A Case Report and Review of the Literature

open access: yesDermatopathology, 2020
Immunoglobulin A (IgA)-mediated leukocytoclastic vasculitis is a cutaneous small-vessel vasculitis characterized by skin findings of palpable purpura. It may occur secondary to infections, neoplasms, drugs, and systemic conditions, although it is most ...
Pallavi Basu   +3 more
doaj   +1 more source

Cutaneous leukocytoclastic vasculitis associated with verapamil and atorvastatin: A case report

open access: yesClinical Case Reports, 2023
Key Clinical Message We report a case of biopsy‐proven cutaneous leukocytoclastic vasculitis developing 10 days after starting verapamil and atorvastatin in a patient with long‐standing Sjogren's syndrome.
Yi Tong Vincent Aw   +1 more
doaj   +1 more source

Cutaneous vasculitis and vasculopathy in the era of COVID-19 pandemic

open access: yesFrontiers in Medicine, 2022
Cutaneous vasculitides encompass a heterogeneous group of clinicopathological entities, which may occur as single-organ vasculitis of the skin or present as skin-limited variant of systemic vasculitis (i.e., skin-limited ANCA-associated vasculitis), and ...
Carlo Alberto Maronese   +11 more
doaj   +1 more source

The histopathological spectrum of acute generalized exanthematous pustulosis (AGEP) and its differentiation from generalized pustular psoriasis [PDF]

open access: yes, 2010
Background: Acute generalized exanthematous pustulosis (AGEP) represents a severe, acute, pustular skin reaction that is most often induced by drugs. AGEP can be difficult to differentiate from generalized pustular psoriasis (GPP) both clinically and ...
Austin   +34 more
core   +11 more sources

Clinic manifestations in granulomatosis with polyangiitis [PDF]

open access: yes, 2016
Granulomatosis with polyangiitis (GPA), formerly Wegener's granulomatosis (WG), is an uncommon immunologically mediated systemic small-vessel vasculitis that is pathologically characterised by an inflammatory reaction pattern (necrosis, granulomatous ...
De Vincentiis, Marco   +7 more
core   +1 more source

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