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先天性的系统性毛细血管漏综合征:皮肤受累被误诊
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作者 fardet l. Kerob D. +2 位作者 Rybojad M. C. lebbé 田中伟 《世界核心医学期刊文摘(皮肤病学分册)》 2005年第4期28-29,共2页
Background: Systemic capillary leak syndrome (SCLS) is a severe disorder characterized by unexplained rapid transferof considerable volumes of plasma from the intravascular to the extravascular compartment. For some c... Background: Systemic capillary leak syndrome (SCLS) is a severe disorder characterized by unexplained rapid transferof considerable volumes of plasma from the intravascular to the extravascular compartment. For some cases of SCLS, no aetiology is evident and these cases are reported as idiopathic (ISCLS). Objectives: To describe the cutaneous findings in 3 patients with ISCLS. Results: Cutaneous involvement consisted in sclerosis, livedo, purpura and photodistributed maculopapular erythematous rash. Dermal mucinosis was proven by biopsy in 1 patient. No underlying disease was diagnosed during follow-up. Conclusion: The above-mentioned cutaneous findings can be present during acute attacks of ISCLS.They seem specifically related to the ISCLS and not indicative of an underlying disease. 展开更多
关键词 急性发作期 斑丘疹 潜在疾病 青斑 外腔 黏蛋白 活组织检查 病因学
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