Makley J T, Carter J R
Clin Orthop Relat Res. 1986 Mar(204):37-44.
Eosinophilic granuloma of bone as a component of the syndrome histiocytosis X is discussed with respect to clinical, pathologic, and radiologic diagnostic biases and discrepancies employing illustrative case material. The subject is reviewed in historical perspective selectively, with emphasis on those features that may serve as a valuable resource in evaluating initial patient presentations and subsequent follow-up evaluation. Salient pathologic and pathogenetic considerations especially germane to clinical phenomena are reviewed, and current therapeutic modalities are summarized.
本文利用实例材料,就作为组织细胞增多症X综合征组成部分的骨嗜酸性肉芽肿在临床、病理及放射学诊断方面的偏差与差异进行了讨论。本文有选择地从历史角度对该主题进行了回顾,重点关注那些在评估患者初始表现及后续随访评估中可能具有重要价值的特征。对与临床现象密切相关的突出病理及发病机制方面的因素进行了回顾,并总结了当前的治疗方式。