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1. シェーグレン症候群の臨床症状：腺外型疾患および予後 clinical manifestations of sjogrens syndrome extraglandular disease and prognosis
2. 成人における免疫性（特発性）血小板減少性紫斑病の臨床症状および診断 clinical manifestations and diagnosis of immune idiopathic thrombocytopenic purpura in adults
3. 成人の特発性皮膚小血管性血管炎患者の管理 management of adults with idiopathic cutaneous small vessel vasculitis
4. 小児における紫斑の評価 evaluation of purpura in children
5. ヘノッホ・シェーンライン紫斑病の臨床症状および診断 clinical manifestations and diagnosis of henoch schonlein purpura

Overexpression of RORγt under control of the CD2 promoter induces polyclonal plasmacytosis and autoantibody production in transgenic mice.

Yoh K, Morito N, Ojima M, Shibuya K, Yamashita Y, Morishima Y, Ishii Y, Kusakabe M, Nishikii H, Fujita A, Matsunaga E, Okamura M, Hamada M, Suto A, Nakajima H, Shibuya A, Yamagata K, Takahashi S.SourceDepartment of Nephrology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan. k-yohnpr@umin.ac.jp
European journal of immunology.Eur J Immunol.2012 Aug;42(8):1999-2009. doi: 10.1002/eji.201142250. Epub 2012 Jul 9.
Retinoic acid related orphan receptor gamma-t (RORγt) is known to be a master regulator of Th17-cell development. In this study, we generated RORγt-overexpressing transgenic (RORγt Tg) mice in which transgene expression was driven by the CD2 promoter, and found that these mice developed polyclona
PMID 22623033

Primary benign hypergammaglobulinemic purpura of Waldenstrom masquerading as disseminated Schamberg's purpura.

Nikam BP, Singh NJ, Shetty DD.
Indian journal of dermatology, venereology and leprology.Indian J Dermatol Venereol Leprol.2011 Mar-Apr;77(2):205-8. doi: 10.4103/0378-6323.77470.
PMID 21393959

Cutaneous macroglobulinosis deposits in a patient with IgM paraproteinemia/incipient Waldenström macroglobulinemia.

Lüftl M, Sauter-Jenne B, Gramatzki M, Eckert F, Jenne L.SourceDermatohistopathological Laboratory, Munich, Germany. lueftl@derma-muenchner-freiheit.de
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.J Dtsch Dermatol Ges.2010 Dec;8(12):1000-3. doi: 10.1111/j.1610-0387.2010.07392.x.
A 43-year-old healthy patient developed disseminated flat skin-colored to red-brown papules over a few months. These papules were the result of cutaneous IgM deposits representing the first symptom of a hitherto undiagnosed IgM paraproteinemia. This extremely rare skin manifestation of IgM paraprote
PMID 20202045

森昌朋 [他],片貝重之,吉羽宣男,松下正也,遠藤恒,田中瑞江,金井君江,田中昌輝,大野忠良,今井貴子,飯塚春太郎,斉藤公司,笛木隆三,小林節雄
日本内科学会雑誌 65(4), 347-353, 1976
… 線像上空洞異常陰影を認め,超遠心像ではmacroglobulin, intermediate complexは証明されず,骨髄の形質細胞も正常であり, pyroglobulin, cryoglobulin,も認められず,出血凝固能検査ではRumpel-Leede現象を除いて正常であつたので, purpura hyperglobulinemicaと診断した1例を経験した.本症例は開胸生検により著しい形質細胞浸潤を伴う慢性気管支炎および肺膿瘍,と判明したので,この病態が長年月にわたる遷延感作の状態を形成し,高ガンマグロブリ …
NAID 130000889995