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Primary cutaneous nodular amyloidosis: case report and review of the literature.

机译:原发性皮肤结节性淀粉样变性病:病例报告和文献复习。

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摘要

Primary cutaneous nodular amyloidosis (PCNA) is a rare form of primary cutaneous amyloidosis. It presents as waxy yellow-red nodules that are located preferentially on the lower extremities, face, scalp, and genitals. Recognition of this condition is of particular importance, as primary systemic amyloidosis can have a similar cutaneous presentation. We report a case of PCNA in a 52-year-old woman with systemic lupus erythematosus (SLE) and Sjogren syndrome (SS). We discuss the need to evaluate for systemic disease and provide a concise review of the literature focusing on clinical presentation, disease associations, and management.
机译:原发性皮肤结节性淀粉样变性病(PCNA)是原发性皮肤性淀粉样变性病的一种罕见形式。它呈蜡状黄红色结节,优先位于下肢,面部,头皮和生殖器上。由于原发性系统性淀粉样变性病可能具有相似的皮肤表现,因此识别这种情况尤为重要。我们报告一名患有系统性红斑狼疮(SLE)和Sjogren综合征(SS)的52岁女性的PCNA病例。我们讨论了评估全身性疾病的必要性,并简要介绍了侧重于临床表现,疾病关联和管理的文献。

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