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原发性骨髓纤维化是一种病因未明的骨髓纤维组织增生性疾病。我院近年来先后收治4例,现报告于下。病例介绍例1:李某某,男,65岁,汉族,干部,住院号103295。患者于10年前体检发现肝脾肿大,多次肝功检查无异常。近年来,自感乏力,食欲减退,面色逐渐苍白,于1977年5月入院。既往体健,否认有化学毒物或放射线接触史。家族史无特殊。体检:呈轻度贫血貌,肝在右肋下2厘米,表面光滑,中等硬度。脾肋下3厘米。余未发现阳性体征。实验室检查:血红蛋白10克％,红细胞344万,白细胞12,400,分类:原粒4％,早幼粒19％,中
Primary myelofibrosis is a myeloproliferative disease of unknown etiology. In recent years, our hospital has admitted 4 cases, the report is now under. Case introduction Example 1: Lee Moumou, male, 65 years old, Han nationality, cadre, hospital number 103295. 10 years ago, patients found liver and spleen enlargement examination, multiple liver function tests were normal. In recent years, self-feeling fatigue, loss of appetite, pale gradually, admitted in May 1977. Past physical health, denied chemical poison or radiation exposure history. No special family history. Physical examination: mild anemia appearance, liver in the right rib 2 cm, smooth surface, medium hardness. Spleen ribs 3 cm. I did not find positive signs. Laboratory tests: hemoglobin 10 g%, red blood cells 344 million, white blood cells 12,400, Category: 4% of the original particles, promyelocytic 19%, medium