Fenyk J R, Smith C M, Warkentin P I, Krivit W, Goltz R W, Neely J E, Nesbit M E, Ramsay N K, Coccia P F, Kersey J H
Lancet. 1978 Mar 4;1(8062):472-3. doi: 10.1016/s0140-6736(78)90136-8.
A female patient with severe idiopathic aplastic anaemia received a successful bone-marrow transplant from her HLA-identical, mixed-lymphocyte-culture-compatible, brother. 8 months after transplantation she had localised cutaneous measles. Chronic sclerodermatous changes developed which were indistinguishable from chronic graft-versus-host disease and were limited to the areas of the original exanthem. Interaction between viral infection and minor histocompatibility differences probably resulted in graft-versus-host disease in this patient.
一名患有严重特发性再生障碍性贫血的女性患者接受了来自其 HLA 相同、混合淋巴细胞培养相容的兄弟的成功骨髓移植。移植后 8 个月,她出现了局限性皮肤麻疹。随后出现了慢性硬皮病样改变,与慢性移植物抗宿主病难以区分,且局限于原来皮疹的部位。病毒感染与次要组织相容性差异之间的相互作用可能导致了该患者发生移植物抗宿主病。