硬皮病患者的原发性局限性皮肤淀粉样变 - Suppr

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超能文献

Primary localized cutaneous amyloidosis in patients with scleroderma.

作者信息

Kikuchi Nobuyuki, Sakai Erika, Nishibu Akiko, Ohtsuka Mikio, Yamamoto Toshiyuki

出版信息

Acta Derm Venereol. 2010 May;90(3):326-7. doi: 10.2340/00015555-0855.

DOI:10.2340/00015555-0855

PMID:20526567

Abstract

摘要

相似文献

Primary localized cutaneous amyloidosis in patients with scleroderma.硬皮病患者的原发性局限性皮肤淀粉样变

Acta Derm Venereol. 2010 May;90(3):326-7. doi: 10.2340/00015555-0855.

A case of sclerodermatomyositis with cutaneous amyloidosis.1例硬皮病样皮肌炎合并皮肤淀粉样变病。

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Primary localised cutaneous amyloidosis in systemic sclerosis.系统性硬化症中的原发性局限性皮肤淀粉样变

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[Truss-induced macular amyloidosis].[疝托诱导性黄斑淀粉样变]

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Light chain multiple myeloma with peripheral leucocytosis presenting as scleroderma amyloidosum of the Alambda-type.伴有外周血白细胞增多的轻链型多发性骨髓瘤，表现为λ型淀粉样硬皮病。

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Nodular primary localized cutaneous amyloidosis.结节性原发性局限性皮肤淀粉样变性

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[Progressive sclerodermia and skin amyloidosis].[进行性硬皮病与皮肤淀粉样变性]

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Diffuse biphasic cutaneous amyloidosis.弥漫性双相性皮肤淀粉样变

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Actas Dermosifiliogr. 2012 Mar;103(2):161-2. doi: 10.1016/j.ad.2011.05.017. Epub 2011 Aug 31.

[Atopic dermatitis with persistent reaction to light and primary cutaneous amyloidosis].[对光持续反应的特应性皮炎与原发性皮肤淀粉样变]

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Acta Derm Venereol. 2024 Jun 8;104:adv40419. doi: 10.2340/actadv.v104.40419.

Clinical and Histopathological Features of Scleroderma-like Disorders: An Update.硬皮病样疾病的临床和组织病理学特征：更新。

Medicina (Kaunas). 2021 Nov 20;57(11):1275. doi: 10.3390/medicina57111275.

Primary Localized Cutaneous Nodular Amyloidosis and Limited Cutaneous Systemic Sclerosis: Additional Cases with Dermatoscopic and Histopathological Correlation of Amyloid Deposition.原发性局限性皮肤结节性淀粉样变与局限性皮肤系统性硬化症：更多伴有淀粉样沉积的皮肤镜和组织病理学相关性病例

Dermatopathology (Basel). 2021 Jul 2;8(3):229-235. doi: 10.3390/dermatopathology8030028.

Primary cutaneous amyloidosis associated with autoimmune hepatitis-primary biliary cirrhosis overlap syndrome and Sjögren syndrome: A case report.原发性皮肤淀粉样变合并自身免疫性肝炎-原发性胆汁性肝硬化重叠综合征及干燥综合征：一例报告

Medicine (Baltimore). 2018 Feb;97(8):e0004. doi: 10.1097/MD.0000000000010004.

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