• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Primary systemic amyloidosis associated with multiple myeloma.

作者信息

Oliveira Ederson Valei Lopes de, Pozetti Ana Carolina Garcia, Pozetti Eurides Maria de Oliveira, Antonio João Roberto, Michalany Nilceo Schwery

机构信息

Medical School, Faculdade de Medicina de São José do Rio Preto, SP, Brazil.

出版信息

An Bras Dermatol. 2012 Jan-Feb;87(1):119-22. doi: 10.1590/s0365-05962012000100015.

DOI:10.1590/s0365-05962012000100015
PMID:22481660
Abstract

This case report is about a 48-year-old female patient with systemic amyloidosis and multiple myeloma simultaneously. Amyloid cutaneous infiltrative lesions like papules, nodules, or plaques with a serous-hemorrhagic aspect were found in the eyelids, neck and retroauricular region, among others. She had presented intermittent papular lesions on the upper eyelids one year before, which worsened following local trauma. A local skin biopsy showed amorphous and eosinophilic substance in the dermis. Congo red staining confirmed the amyloid deposits. Abnormal exams: proteinuria (570 mg/24h), Bence-Jones proteinuria and clonal plasma cells (70%) found in myelogram. Following the diagnosis of multiple myeloma based on amyloid skin lesions, the patient was referred to the Hematology service and died 5 months after the diagnosis.

摘要

相似文献

1
Primary systemic amyloidosis associated with multiple myeloma.
An Bras Dermatol. 2012 Jan-Feb;87(1):119-22. doi: 10.1590/s0365-05962012000100015.
2
Bence-Jones protein-type myeloma with amyloid myopathy presenting as amyloidomas and extensive amyloid deposits in the muscularis propria: a rapidly fatal autopsy case.伴淀粉样肌病的本-周蛋白型骨髓瘤,表现为淀粉样瘤及固有肌层广泛淀粉样沉积:1例快速致死的尸检病例
Int J Surg Pathol. 2012 Feb;20(1):83-8. doi: 10.1177/1066896911410690. Epub 2011 Jun 1.
3
The blue man: a novel cutaneous manifestation of systemic amyloidosis.蓝色人:系统性淀粉样变性的一种新的皮肤表现。
Amyloid. 2011 Sep;18(3):156-9. doi: 10.3109/13506129.2011.571318. Epub 2011 Apr 20.
4
[Bullous amyloidosis].[大疱性淀粉样变]
Rinsho Ketsueki. 1993 Sep;34(9):1050-2.
5
Primary systemic amyloidosis with delayed progression to multiple myeloma.原发性系统性淀粉样变性伴进展为多发性骨髓瘤延迟。
Cancer. 1998 Apr 15;82(8):1501-5.
6
Amyloid deposition of systemic myeloma-associated amyloidosis excludes actinic elastotic material.系统性骨髓瘤相关淀粉样变性的淀粉样沉积不包括光化性弹性组织变性物质。
Eur J Dermatol. 2002 Nov-Dec;12(6):607-8.
7
Lichen amyloidosis in an unusual location.罕见部位的苔藓样淀粉样变。
Singapore Med J. 2007 Jun;48(6):e165-7.
8
Perianal condyloma-like lesions in multiple myeloma associated amyloidosis.多发性骨髓瘤相关淀粉样变性中的肛周尖锐湿疣样病变
Eur J Dermatol. 2004 May-Jun;14(3):193-5.
9
Spontaneous bilateral peri-orbital purpura: an important clinical sign of primary systemic amyloidosis.自发性双侧眶周紫癜:原发性系统性淀粉样变性的重要临床体征。
BMJ Case Rep. 2021 Apr 1;14(4):e239478. doi: 10.1136/bcr-2020-239478.
10
IgD myeloma with myelofibrosis and amyloidosis.伴有骨髓纤维化和淀粉样变性的IgD骨髓瘤
Arch Pathol Lab Med. 1977 Jan;101(1):10-3.

引用本文的文献

1
When the Skin Speaks: Dermatological Clues in Multiple Myeloma.当皮肤“开口”:多发性骨髓瘤的皮肤学线索
Indian Dermatol Online J. 2025 Jan 20;16(4):622-625. doi: 10.4103/idoj.idoj_332_24. eCollection 2025 Jul-Aug.
2
Primary systemic amyloidosis, acquired cutis laxa and cutaneous mucinosis in a patient with multiple myeloma.一名多发性骨髓瘤患者出现原发性系统性淀粉样变性、获得性皮肤松弛症和皮肤黏液瘤病。
An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):32-5. doi: 10.1590/abd1806-4841.20132531.