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遗传性椭园形红细胞增多症是一种少见的血液病,呈常染色体显性遗传。现将我院收治的1例报告如下: 女患,50岁,汉族,病案号:122870,因重度贫血于1983年5月19日入院。生于黑龙江省,1968年体检发现肝于右肋弓下3.0cm,未给予治疗。近三年来有时四肢皮肤见少量淤斑,今年四月末突然呕血约500ml,血色暗红,在当地医院诊断为上消化道出血。
Hereditary polycythemia is a rare blood disease, autosomal dominant. A case report from our hospital is as follows: Female patient, 50 years old, Han nationality, case number: 122870, admitted to hospital on May 19, 1983 due to severe anemia. Born in Heilongjiang Province, 1968 physical examination found that the liver in the right costal arch 3.0cm, did not give treatment. In the past three years, sometimes the skin of the extremities has seen a small amount of ecchymosis. At the end of April this year, there was a sudden vomiting of about 500ml and dark redness. It was diagnosed as upper gastrointestinal bleeding in a local hospital.