Ysebaert L, Deconinck E, Larosa F, Caillot D, Tiberghien P, Casasnovas R O, Cahn J Y
Service d'Hématologie, CHU Bocage, Dijon, France.
Bone Marrow Transplant. 2002 May;29(10):873-4. doi: 10.1038/sj.bmt.1703560.
A case of polyarteritis is reported in an 18-year old woman, occurring 2 years after an allogeneic bone marrow transplant. The clinical manifestations were similar to those of polyarteritis nodosa (PAN) with a wide range of organs involved including life-threatening cardiac and mesenteric problems requiring plasmapheresis and intravenous immunoglobulin (IgIV).
一名18岁女性在接受异基因骨髓移植2年后发生了一例多动脉炎。临床表现与结节性多动脉炎（PAN）相似，累及多个器官，包括危及生命的心脏和肠系膜问题，需要进行血浆置换和静脉注射免疫球蛋白（IgIV）。
