Vasculitis
☆ Tamin'ny valin'ny Stiftung Warentest 2022 avy any Alemaina, ny fahafaham-pon'ny mpanjifa amin'ny ModelDerm dia ambany kely noho ny fifampidinihana telemedicine karama.
Fikorontanan'ny rafitra hafa (aretin'ny autoimmune) misy vasculitis dia tokony hofoanana.
Ity dia sary mahazatra amin'ny vasculitis amin'ny tongotra. Azo atao ny fitsirihana ny urine mba hijerena ny tsy fahatomombanana amin'ny fiasan'ny voa.
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 dia karazana fivontosana hoditra miantraika amin'ny lalan-drà kely ao anaty sosona lalina amin'ny hoditra. Mety hitranga tsy misy antony izany na mifandray amin'ny aretina, fivontosana, aretina autoimmune, na fanafody. Ny famantarana mahazatra dia ahitana tasy mena na volomparasy amin'ny tongotra, fidiran'ny sambo kely, ary amin'ny 30 isan-jaton'ny tranga dia misy faritra hafa amin'ny vatana ihany koa. Ny ankamaroan'ny tranga dia mivaha irery ao anatin'ny herinandro vitsivitsy na volana vitsivitsy. Ny fitsaboana dia miovaova arakaraka ny hamafin'izany, manomboka amin'ny fampihenana tsikelikely ny corticosteroids am-bava mankany amin'ny fampiasana fanafody hafa izay mampihena ny areti-maso tsy misy steroid.
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.
○ Diagnose
Ny vasculitis voafetra amin'ny hoditra dia mety hihatsara rehefa mandeha ny fotoana. Na izany aza, azo atao ny fitiliana ra sy urine mba hamantarana ny aretin'ny rafitra na ny autoimmune.
○ Fitsaboana - Fanafody OTC
Raha toa ka voafetra amin'ny hoditra ny vasculitis nefa tsy miditra amin'ny taova hafa, dia azo ampiasaina ny menaka steroid.
#OTC steroid ointment