Kan'shina N F, Matsko D E
Arkh Patol. 1978;40(12):57-61.
A case of hemolytic-uremic syndrome (Gasser syndrome) in a boy of 7 is described. The disease was accompanied by thrombocytopenia, anemia, hemorrhagic syndrome and acute renal insufficiency (ARI). Morphological lesions consisted in the predominant involvement of the kidneys presenting thrombosis of the glomerular capillaries and reglomerular arterioles, fine cortical necroses, and considerable degenerative changes in the tubular epithelium. The peculiar features of the disease included low intensity of hemolysis and the lack of the oligoanuric phase of ARI.
本文描述了一名7岁男孩患溶血性尿毒症综合征（加塞尔综合征）的病例。该疾病伴有血小板减少、贫血、出血综合征和急性肾功能不全（ARI）。形态学病变主要表现为肾脏受累，出现肾小球毛细血管和小叶间动脉血栓形成、皮质微小坏死以及肾小管上皮细胞的明显退行性改变。该疾病的独特特征包括溶血强度低以及缺乏ARI的少尿期。
