Immunoglobulins and C3 were detected by immunoflourescence in the blood vessel walls of biopsies of clinically normal skin in patients with active necrotizing vasculitis. Of the 13 patients studied, 9 had C3 and 6 of these had IgM or IgA in biopsies of lesions of vasculitis. In adjacent clinically normal skin, 7 patients had C3 and 3 of these also had IgM or IgA. These findings support the hypothesis that immunoglobulins and complement are present in vessels of some patients prior to chemotaxis of polymorphonuclear leukocytes and the resulting inflammatory purpuric lesions so characteristic of necrotizing vasculitis
A 62-year-old man was diagnosed with IgG4-related disease based on multiple sites of lymphadenopathy...
Previous immunofluorescent studies showing deposits of immunoglobulin and complement at the cutaneou...
Cutaneous leukocytoclastic vasculitis is characterized by the deposition of circulating immune compl...
To study the mechanisms responsible for Ieukocytoclastic vasculitis, we evaluated the kinetics of im...
Systemic vasculitides are a group of rare diseases characterized by inflammation of the arterial or ...
Systemic vasculitides are a group of rare diseases characterized by inflammation of the arterial or ...
Systemic vasculitides are a group of rare diseases characterized by inflammation of the arterial or ...
Antineutrophil cytoplasmic autoantibodies (ANCA) are the likely cause for necrotizing small vessel v...
Antineutrophil cytoplasmic autoantibodies (ANCA) are the likely cause for necrotizing small vessel v...
Systemic vasculitides are a group of uncommon diseases characterized by blood vessel inflammation. T...
A 62-year-old man was diagnosed with IgG4-related disease based on multiple sites of lymphadenopathy...
IgA-vasculitis is a systemic small-vessel leucocytoclastic vasculitis and is associated with a high ...
IgA-vasculitis is a systemic small-vessel leucocytoclastic vasculitis and is associated with a high ...
The specificity and incidence of deposits of immunoglobulin and complement in the walls of vessels i...
Necrotising vasculitis is a very rare occurrence and commonly caused by an underlying autoimmune pat...
A 62-year-old man was diagnosed with IgG4-related disease based on multiple sites of lymphadenopathy...
Previous immunofluorescent studies showing deposits of immunoglobulin and complement at the cutaneou...
Cutaneous leukocytoclastic vasculitis is characterized by the deposition of circulating immune compl...
To study the mechanisms responsible for Ieukocytoclastic vasculitis, we evaluated the kinetics of im...
Systemic vasculitides are a group of rare diseases characterized by inflammation of the arterial or ...
Systemic vasculitides are a group of rare diseases characterized by inflammation of the arterial or ...
Systemic vasculitides are a group of rare diseases characterized by inflammation of the arterial or ...
Antineutrophil cytoplasmic autoantibodies (ANCA) are the likely cause for necrotizing small vessel v...
Antineutrophil cytoplasmic autoantibodies (ANCA) are the likely cause for necrotizing small vessel v...
Systemic vasculitides are a group of uncommon diseases characterized by blood vessel inflammation. T...
A 62-year-old man was diagnosed with IgG4-related disease based on multiple sites of lymphadenopathy...
IgA-vasculitis is a systemic small-vessel leucocytoclastic vasculitis and is associated with a high ...
IgA-vasculitis is a systemic small-vessel leucocytoclastic vasculitis and is associated with a high ...
The specificity and incidence of deposits of immunoglobulin and complement in the walls of vessels i...
Necrotising vasculitis is a very rare occurrence and commonly caused by an underlying autoimmune pat...
A 62-year-old man was diagnosed with IgG4-related disease based on multiple sites of lymphadenopathy...
Previous immunofluorescent studies showing deposits of immunoglobulin and complement at the cutaneou...
Cutaneous leukocytoclastic vasculitis is characterized by the deposition of circulating immune compl...