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垂体柄郎罕氏细胞增多症(附1例报告及文献复习) 被引量:1

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摘要 郎罕氏细胞增多症(Langerhang’Cell Histiocytosis LCH)是一种孤立性的组织细胞的非肿瘤性质的异常分化,过去称为组织细胞增生症X(Histiocytosis X)。LCH临床表现复杂,为一系列临床症候群。MRI及CT表现无特异性。病理有特异的形态学和免疫组织化学特征,是确诊的唯一金指标。治疗为药物和手术治疗,依病情拟定治疗方案。根据病理损害程度及患者年龄、性别等,预后不同。
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2008年第21期1226-1227,共2页 Chinese Journal of Clinical Oncology
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参考文献7

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二级参考文献7

  • 1黄兆民,肖官惠,陈君禄,庄文权,卢剑武,陈应明,孟恢非.骨嗜酸性肉芽肿的放射学诊断(附60例分析)[J].中华放射学杂志,1995,29(6):397-400. 被引量:53
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