医学
无症状的
阿那格雷内酯
弱点
免疫抑制
强的松
外科
皮肤病科
活检
腹部
环磷酰胺
介绍(产科)
病理
内科学
化疗
血小板
原发性血小板增多症
作者
Lauren Schaefer,Theresa Wampler Muskardin,Jan‐Mendelt Tillema,Carilyn N. Wieland,Megha M. Tollefson
摘要
Abstract A 17‐year‐old Caucasian boy presented with progressive left‐sided weakness, transient slurred speech, and skin lesions characterized by 3‐5 mm, pink, asymptomatic papules with white atrophic centers on his central abdomen, back, and lower extremities. Skin biopsy confirmed the diagnosis of malignant atrophic papulosis, a rare vasculopathy that leads to the occlusion of small‐ and medium‐sized arteries. He was treated with cyclophosphamide, eculizumab, treprostinil, pentoxifylline, heparin, and acetylsalicylic acid. Despite the aggressive immunosuppression, humanized monoclonal antibodies, and antiplatelet therapy, he died two months after presentation. We report this case to highlight diagnostic features, as well as to highlight the importance of early diagnosis and treatment.
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