首页> 外文期刊>Dermatologica Sinica >Purpuric halo around hemangioma as a clue for primary systemic amyloidosis: Case report and review of literature
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Purpuric halo around hemangioma as a clue for primary systemic amyloidosis: Case report and review of literature

机译:血管瘤周围的紫癜光晕作为原发性系统性淀粉样变性病的线索:病例报告和文献复习

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Mucocutaneous lesion appears in up to 40% of patients with primary systemic amyloidosis (AL amyloidosis). The cutaneous signs may be co-expressed with other organ involvement or even solely presented as the first clue. We reported a case of systemic AL amyloidosis who was initially presented as a solitary hemangioma with a purpuric halo. Excisional biopsy revealed a hemangioma with amyloid deposited in thickened vascular walls. Systemic AL amyloidosis was diagnosed after thorough survey. The stage of disease at the time of initial treatment is the greatest prognostic factor. To our knowledge, this is the first case of systemic AL amyloidosis initially presented as a purpuric halo around hemangioma in Taiwan. This target-like lesion should be linked to systemic AL amyloidosis and early diagnosis is extraordinary important.
机译:多达40%的原发性系统性淀粉样变性病(AL淀粉样变性)患者出现粘膜皮肤病变。皮肤体征可能与其他器官受累共表达,甚至仅作为第一个线索出现。我们报告了一例全身性AL淀粉样变性病,该病例最初表现为孤立性血管瘤伴紫癜性晕圈。切除活检显示血管瘤,淀粉样蛋白沉积在增厚的血管壁上。全面检查后诊断为系​​统性AL淀粉样变性。初始治疗时的疾病阶段是最大的预后因素。据我们所知,这是台湾地区首例全身性AL淀粉样变性病,最初表现为血管瘤周围的紫癜性晕圈。这种目标样病变应与全身性AL淀粉样变性有关,早期诊断非常重要。

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