Wroble R R, Weinstein S L
Department of Orthopaedics, University of Iowa Hospitals, Iowa City 52242.
J Pediatr Orthop. 1988 Mar-Apr;8(2):213-8.
Histiocytosis X can exhibit a variety of musculoskeletal manifestations. Nonetheless, this case exhibits two striking features. Severe progressive scoliosis and massive osteolysis of both femoral shafts occurred in conjunction with the Hand-Schüller-Christian form of histiocytosis X. The scoliosis was treated successfully by posterior fusion and instrumentation. The clinical features of histiocytosis X are reviewed. Speculation as to the etiology of these features is presented.
组织细胞增多症X可表现出多种肌肉骨骼表现。尽管如此，该病例呈现出两个显著特征。严重进行性脊柱侧弯和双侧股骨干大量骨质溶解与汉-许-克氏组织细胞增多症X型同时出现。脊柱侧弯通过后路融合和器械固定成功治疗。对组织细胞增多症X的临床特征进行了综述。并对这些特征的病因进行了推测。
