期刊文献+

结节型皮肤淀粉样变性

Nodular cutaneous amyloidosis: report of two cases
下载PDF
导出
摘要 报告2例结节型皮肤淀粉样变性。例1.男,61岁。右下颌蚕豆大红色斑块1年。例2.女,64岁。左腘窝两枚蚕豆至鸡蛋大的黄红色斑块30余年。皮肤组织病理检查提示表皮萎缩,真皮全层可见淡红色结节状均一物质沉积,结晶紫染色阳性。诊断为结节型皮肤淀粉样变性。 Two cases of nodular cutaneous amyloidosis are reported. Case 1. A 61-year-old man presented with a broad bean-sized, red nodule on the right side of the mandible. Case 2. A 64-year-old woman presented with two yellowish red color plaques, sized from bean to egg on the left popliteal fossa. Histopathological examination showed atrophy of the epider- mis, some reddish, deposits of homogeneous nodular substance, and lymphocytes and plasma ceils were infiltrated in the whole layer of the dermis. Crystal violet staining was positive. The diagnosis of nodular cutaneous amyloidosis was made.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2015年第6期377-379,共3页 Journal of Clinical Dermatology
关键词 淀粉样变性 结节型 皮肤 amyloidosis, nodular, cutaneous
  • 相关文献

参考文献5

  • 1Tong PL, Walker WA, Glancy RJ, et al. Primary localized cutaneous nodular amyloidosis successfully treated with cyclophosphamide [J]. Australas J Dermatol, 2013, 54(1): 12-15.
  • 2Lee DY, Kim YJ, Lee JY, et al. Primary localized cutaneous nodular amyloidosls following local trauma[J]. Ann Dermatol, 2011, 4(23): 515-518.
  • 3Kakani RS, Goldstein AE, Meisher I, et al. Nodular amyloidosis: case report and literature review[J]. J Cutan Med Surg, 2001, 5 (2): 101-104.
  • 4周静,袁肖海,宋宁静.原发性皮肤结节型淀粉样变性[J].临床皮肤科杂志,2013,42(1):29-30. 被引量:2
  • 5Lai KW, Lambert E, Coleman S, et al. Nodular amyloidosis: differentiation from colloid milium by electron microscopy[J]. Am J Dermatopathol, 2009, 5(31): 472-474.

二级参考文献12

  • 1顾俊瑛,陈明华,肖丽明,李晓建.结节性皮肤淀粉样变性一例[J].国际皮肤性病学杂志,2006,32(5):270-272. 被引量:3
  • 2McKee PH,Granter SR,Calonje E.皮肤病理学——与临床的联系[M].3版.朱学骏,孙建方,译.北京:北京大学医学出版社,2007:1711.
  • 3Summers EM, Kendriek CG. Primary. localized cutaneous nodular amyloidosis and CREST syndrome; a case report and review of the literature[J]. Cutis, 2008, 82(1): 55-59.
  • 4Kalajian AH, Waldman M, Knable AL. Nodular primary localized cutaneous amyloidosis after trauma: a case report and discussion of the rate of progression to systemic amyloidosis[J]. J Am Acad Dermatol, 2007, 57(2): 26-29.
  • 5Schwendiman MN, Beachkofsky TM, Wisco QJ, et al. Primary cutaneous nodular amyloidosis: case report and review of the lit- erature[J]. Cutis, 2009, 84(2): 87-92.
  • 6Yoneyama K, Tochigi N, Oikawa A, et al. Primary localized cutaneous nodular amyloidosis in a patient with Sjagren's syn- drome: a review of the literature[J]. J Dermatol, 2005, 32(2): 120-123.
  • 7Ueno M, Yamamoto T, Yamanaka M, et al. Nodular amyloidosis in a patient with liver cirrhosis[J]. Dermatol Online J, 2011, 17 (7): 1O.
  • 8Borowicz J, Gillespie M, Miller R. Cutaneous amyloidosis[J]. Skin- reed, 2011, 9(2): 96-100.
  • 9Clos AL, Lasagna-Reeves Ca, Castillo-Carranza DL. Formation of immunoglobulin light chain amyloid oligomers in primary cuta- neous nodular amyloidosis [J]. Br J Dermatol, 2011, 165 (6): 1349-1354.
  • 10Moon AO, Calamia KT, Walsh JS. Nodular amyloidosis: review and long-term follow-up of 16 cases[J]. Arch Dermatol, 2003, 139(9): 1157-1159.

共引文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部