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[原发性皮肤淀粉样变。自然病程]

[Genuine cutaneous amyloidosis. Natural course].

作者信息

Porto J A

出版信息

Med Cutan Ibero Lat Am. 1985;13(1):1-3.

PMID:3887056
Abstract

A case of primary localized cutaneous amyloidosis followed up during 35 years is reported. The initial lesions and the pruritus disappeared after years of evolution and new lesions appeared in other areas. These findings confirm previous observations of the author who reported on 24 patients with primary localized cutaneous amyloidosis followed up for 20 to 30 years. In seven of them amyloid was demonstrated in areas where clinical lesions had disappeared. In most patients either the clinical lesions the pruritus, or both had disappeared and in many patients other clinical lesions had appeared in other locations.

摘要

报告了一例原发性局限性皮肤淀粉样变随访35年的病例。最初的皮损和瘙痒在数年演变后消失,其他部位出现了新的皮损。这些发现证实了作者之前的观察结果,作者曾报告24例原发性局限性皮肤淀粉样变患者,随访20至30年。其中7例在临床皮损消失的部位证实有淀粉样变。大多数患者的临床皮损或瘙痒或两者均消失,许多患者在其他部位出现了其他临床皮损。

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