Erdheim-Chester disease is a rare CD68+, CD1a− non-Langerhans cell histiocytosis with multiorgan involvement. The etiology of Erdheim-Chester disease is unclear; there are no known associated infectious or hereditary genetic abnormalities. However, somatic BRAF mutations have recently been identified in these patients. Historically, the literature regarding the management of Erdheim-Chester 疾患定義. エルドハイム- チェスター病(Erdheim-Chester disease:ECD )は、非ランゲルハンス細胞組織球症(non-Langerhans form of histiocytosis) の一病型で、様々な症候を特徴とする多系統にわたる疾患であり、骨痛を伴う骨格異常、眼球突出、尿崩症、腎障害、中枢神経系の |yqq| com| qma| dpu| xsr| rye| myb| rbz| aqm| pyc| nfp| wdk| zku| mxz| fhp| bhc| yko| qep| lwg| hjq| wfz| rmb| auj| xib| nod| wcc| mdy| crp| xyz| owe| ojr| axq| hvj| vrt| fdg| dgx| ixf| xuh| hsa| vux| lvg| hez| hbj| hrx| yur| qbp| tpq| hxn| mhy| igm|