Kohler T R, Tilney N L
Transplant Proc. 1982 Jun;14(2):444-7.
A patient is described who developed severe microangiopathic hemolytic anemia associated with hyperacute rejection of a maternal renal allograft. The syndrome included profound anemia and thrombocytopenia, refractory to either blood or platelet transfusions, increased plasma hemoglobin levels and the appearance of circulating fibrin split products. All hemotologic abnormalities reversed themselves promptly following graft nephrectomy. The pathophysiology of this infrequent condition is discussed.
本文描述了一名患者，其发生了严重的微血管病性溶血性贫血，与母体肾移植的超急性排斥反应相关。该综合征包括严重贫血和血小板减少，对输血或血小板输注均无效，血浆血红蛋白水平升高以及循环纤维蛋白裂解产物的出现。肾移植切除术后，所有血液学异常迅速自行逆转。本文讨论了这种罕见病症的病理生理学。
