Vasculitis
☆ In anno 2022 Stiftung Warentest ex Germania provenit, satisfactio consumptoria cum ModelDerm paulo minus fuit quam cum consultationibus telemedicinis solutis.
Aliae perturbationes systemicae (morbus autoimmunes) vasculitis involventium excludi debent.
Haec imago typica vasculitis cruris est. Urina test fieri potest ad reprimendam abnormitates in renibus functionis.
References
Of the 61 patients studied, hypersensitivity vasculitis (HSV) [23 (37.7%)] and Henoch Schonlein purpura (HSP) [16 (26.2%)] were the two most common forms. Systemic involvement was seen in 32 (52.45%) patients. Drugs were implicated in 12 (19.7%) cases, infections in 7 (11.4%) and connective tissue disorders in 4 (6.5%) cases. No association was seen between history of drug intake and tissue eosinophilia and also between histologically severe vasculitis and clinical severity.
Leukocytoclastic vasculitis Genus est inflammatio cutis parvae venae sanguineae in stratis profundis cutis. Contingit sine nota ratione vel cum infectionibus, tumoribus, morbis autoimmune vel medicamentis coniungi. Signa typica includunt maculas rubras vel purpureas crurum, implicationem vasculorum, et circiter XXX centesimas casuum, aliae quoque partes corporis afficiuntur. Pleraque aperiunt sua intra paucos septimanas ad menses. Variatur curatio quam vehemens sit, paulatim reducendo corticosteroides orales ut aliis medicamentis, quae inflammatio inferior sine steroidibus utatur.
Leukocytoclastic vasculitis is a cutaneous, small-vessel vasculitis of the dermal capillaries and venules. This condition can be idiopathic or can be associated with infections, neoplasms, autoimmune disorders, and drugs. Key clinical features of leukocytoclastic vasculitis include palpable purpura on the lower extremity, small vessel involvement, and, in about 30 percent of individuals, extracutaneous involvement. Most cases of idiopathic cutaneous, small vessel vasculitis are self-limited with 90 percent of cases resolving in weeks to months of onset. Otherwise, treatment depends on the severity of disease and can range from an oral corticosteroid taper to various steroid-sparing immunosuppressive agents.
Leukocytoclastic vasculitis is a cutaneous, small-vessel vasculitis of the dermal capillaries and venules. This condition can be idiopathic or can be associated with infections, neoplasms, autoimmune disorders, and drugs. Key clinical features of leukocytoclastic vasculitis include palpable purpura on the lower extremity, small vessel involvement, and, in about 30 percent of individuals, extracutaneous involvement. Most cases of idiopathic cutaneous, small vessel vasculitis are self-limited with 90 percent of cases resolving in weeks to months of onset. Otherwise, treatment depends on the severity of disease and can range from an oral corticosteroid taper to various steroid-sparing immunosuppressive agents.
○ Diagnosis
Vasculitis cuti limitata super tempus emendare potest. Sed probatio sanguinis et urinae fieri potest ad perturbationes systemicas vel autoimmunes deprehendendas.
○ Curatio OTC Medicamenta
Si vasculitis limitatur ad cutem sine incursu aliorum organorum, oleum steroidum adhiberi potest.
#OTC steroid ointment