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A Case of Henoch-Schonlein Purpura Developed during Treatment of Lung Cancer / 결핵및호흡기질환
Article in Ko | WPRIM | ID: wpr-58888
Responsible library: WPRO
ABSTRACT
Henoch-Schonlein Purpura (HSP) is a systemic vasculitis involving small vessels with the deposition of immune complexes containing IgA and C3, which is characterized by associated skin, joint, renal, and gastrointestinal manifestations. Although there were several causes such as autoimmunity, infection, and drugs, it also can be presented as a form of vasculitidies associated with malignancies. We report a case of HSP developed during treatment for non-small cell lung cancer in a 66-year-old man. Multiple purpuric skin lesions occurred in both legs after the first cycle of chemotherapy, which was diagnosed as HSP by clinical and pathologic examinations. Due to the itching sensation, topical steroid was applied and the patient was improved 3 weeks later without a scheduled change in chemotherapy.
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Full text: 1 Index: WPRIM Main subject: Pruritus / IgA Vasculitis / Sensation / Skin / Vasculitis / Immunoglobulin A / Autoimmunity / Carcinoma, Non-Small-Cell Lung / Systemic Vasculitis / Joints Limits: Aged / Humans Language: Ko Journal: Tuberculosis and Respiratory Diseases Year: 2009 Type: Article
Full text: 1 Index: WPRIM Main subject: Pruritus / IgA Vasculitis / Sensation / Skin / Vasculitis / Immunoglobulin A / Autoimmunity / Carcinoma, Non-Small-Cell Lung / Systemic Vasculitis / Joints Limits: Aged / Humans Language: Ko Journal: Tuberculosis and Respiratory Diseases Year: 2009 Type: Article