Portal cirrhosis.

J. Mintz
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引用次数: 5

Abstract

cells, 2,050,000; hgb. (Sahli), 45 per cent; white blood cells, 2,400, with polymorphonuclear leucocytes 63 per cent, lymphocytes 31 per cent, mononuclear cells 5 per cent, and eosinophiles 1 per cent. The absolute scarcity of blood platelets precluded an accurate count. Vital staining for reticulocytes revealed only three reticulated erythrocytes after careful search of approximately 12,000 cells. Blood smears revealed erythrocytes of normal size and shape, but with a considerable degree of hypochromia. Bleeding and coagulation times were slightly prolonged. The red cell fragility test was within normal limits, as was the sedimentation rate. The serum calcium level was normal. The capillary resistance test was strongly positive, and it was noted that wherever the finger was punctured a small zone of subdermal heemorrhage resulted. Efforts to determine a toxic factor in this case were unsuccessful. No focus of infection was demonstrable in nose, sinuses, throat, or teeth. The final diagnosis was idiopathic aplastic antemia, with grave prognosis. The patient returned to her home in a distant city on the third day after admission. The therapeutic use of small frequent blood transfusions was recommended to the patient's physician but, in spite of this treatment, she expired within one month. An autopsy was not obtained.
门户肝硬化。
细胞,2050000;hgb。(Sahli),45%;白细胞2400个,多形核白细胞63%,淋巴细胞31%,单核细胞5%,嗜酸性粒细胞1%。血小板的绝对缺乏使计数无法准确。网织红细胞的活力染色在仔细搜索大约12000个细胞后仅显示三个网状红细胞。血涂片显示红细胞大小和形状正常,但有相当程度的低色素。出血和凝血时间略有延长。红细胞脆性测试在正常范围内,沉降率也是如此。血清钙水平正常。毛细管阻力测试呈强阳性,值得注意的是,无论手指在哪里被刺穿,都会产生一小块皮下出血。在本案中,确定毒性因素的努力没有成功。鼻、鼻窦、喉咙或牙齿没有明显的感染灶。最终诊断为特发性再生障碍性贫血,预后严重。患者在入院后的第三天回到了她在一个遥远城市的家中。建议患者的医生使用小规模频繁输血进行治疗,但尽管进行了这种治疗,她还是在一个月内死亡。没有进行尸检。
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