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伴Leiden V因子突变和狼疮抗凝物的恶性萎缩性丘疹病(Degos病)死亡1例
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作者 hohwy t Glü mer Jensen M +1 位作者 tφttrup A. 王琼 《世界核心医学期刊文摘(皮肤病学分册)》 2006年第9期23-24,共2页
Malignant atrophic papulosis (Degos’disease) is a very rare condition characterized by atrophic papular skin lesions and variable association of systemic involvement. We describe a 33-year-old man who presented with ... Malignant atrophic papulosis (Degos’disease) is a very rare condition characterized by atrophic papular skin lesions and variable association of systemic involvement. We describe a 33-year-old man who presented with a widespread skin eruption consistent with malignant atrophic papulosis. During the course of the disease he even developed penile ulcerations, a symptom that has been reported only a few times previously. He subsequently died of multiple perforations of the small bowel 2.5 years after onset of the disease. Laboratory investigations revealed a mutation of factor V Leiden and the presence of lupus anticoagulant, but no anti-cardiolipin antibodies. The patient was treated with narrow-band ultraviolet (UV)B, prednisolone and, later, aspirin, pentoxifyllin and warfarin. Despite this very intensive anti-coagulant and anti-platelet therapy, the treatment had no effect on the skin lesions and could not prevent systemic involvement. 展开更多
关键词 恶性萎缩性丘疹病 DEGOS病 狼疮抗凝物 V因子突变 LEIDEN 抗血小板治疗 抗心肌磷脂抗体 死亡
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