[Systemic plasmacytosis--syndrome of multiple peculiar skin eruptions, lymphadenopathy and polyclonal hypergammaglobulinemia].
作者信息
Watanabe S, Oohara K, Kukita A, Mori S
出版信息
Nihon Hifuka Gakkai Zasshi. 1983 Dec;93(14):1513-26.
PMID:6676500
Abstract
摘要
相似文献
1
[Systemic plasmacytosis--syndrome of multiple peculiar skin eruptions, lymphadenopathy and polyclonal hypergammaglobulinemia].[系统性浆细胞增多症——多种特殊皮肤疹、淋巴结病和多克隆高丙种球蛋白血症综合征]
Nihon Hifuka Gakkai Zasshi. 1983 Dec;93(14):1513-26.
2
Systemic plasmacytosis. A syndrome of peculiar multiple skin eruptions, generalized lymphadenopathy, and polyclonal hypergammaglobulinemia.系统性浆细胞增多症。一种具有独特的多发性皮肤疹、全身性淋巴结病和多克隆高球蛋白血症的综合征。
Arch Dermatol. 1986 Nov;122(11):1314-20. doi: 10.1001/archderm.122.11.1314.
3
[Idiopathic plasmacytic lymphadenopathy with polyclonal hyperimmunoglobulinemia (IPL) characterized by cutaneous involvement].
Rinsho Ketsueki. 1985 Dec;26(12):2021-6.
4
Multicentric Castleman disease with cutaneous manifestations: report of 2 cases and comparison with systemic plasmacytosis.伴有皮肤表现的多中心性Castleman病：2例报告并与系统性浆细胞增多症比较
Dermatology. 2007;214(2):170-3. doi: 10.1159/000098578.
5
Idiopathic plasmacytic lymphadenopathy with polyclonal hypergammaglobulinemia accompanied with cutaneous involvement and renal dysfunction.伴有皮肤受累及肾功能不全的特发性浆细胞性淋巴结病伴多克隆高球蛋白血症
Jpn J Clin Oncol. 2009 Oct;39(10):682-5. doi: 10.1093/jjco/hyp073. Epub 2009 Jul 8.
6
[Two cases of primary cutaneous plasma cytosis--the localized type of primary cutaneous plasmacytosis: a new clinical entity?].
Nihon Hifuka Gakkai Zasshi. 1986 May;96(6):609-16.
7
Bone marrow plasmacytosis in idiopathic plasmacytic lymphadenopathy with polyclonal hyperimmunoglobulinemia: a report of four cases.
Pathol Res Pract. 2007;203(11):789-94. doi: 10.1016/j.prp.2007.08.001. Epub 2007 Sep 27.
8
9
Idiopathic plasmacytic lymphadenopathy with polyclonal gammopathy in a patient of Western origin.
Int J Surg Pathol. 2005 Jan;13(1):125-6. doi: 10.1177/106689690501300121.
10
Immunoblastic lymphadenopathy. A report of two cases.
Arch Pathol Lab Med. 1976 Sep;100(9):465-8.
引用本文的文献
1
Cutaneous plasmacytosis resembling pityriasis rosea in a 66-year-old white woman: A rare disease presenting in an unusual patient demographic.一名66岁白人女性出现类似玫瑰糠疹的皮肤浆细胞增多症：一种在不寻常患者群体中出现的罕见疾病。
JAAD Case Rep. 2017 Feb 4;3(1):78-81. doi: 10.1016/j.jdcr.2016.11.008. eCollection 2017 Jan.
Zotero 插件