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骨嗜酸性肉芽肿是原发于骨髓腔,以组织细胞及嗜酸性白细胞为主要结构特征的肉芽组织样病变。本病首先由Lichtenstein(1940)报告并命名,继后认为本病与Hand-Schuller-Christian氏病,Letter-er-Siwe氏病三者是临床表现不同而有共同病理基础的网状内皮细胞增生性疾病,共同命名为组织细胞病X。本病临床较为少见,国内仅见个案报告。现将我院1973～1989年间收治并经病理组织学证实的眼眶骨嗜酸性肉芽肿7例,就其临床表现与治疗情况分析讨论。
Eosinophilic granulomatous is the primary bone marrow cavity in order to organize cells and eosinophils as the main structural features of granulation tissue-like lesions. The disease was first reported and named by Lichtenstein (1940), then that the disease and Hand-Schuller-Christian’s disease, Letter-er-Siwe’s disease is a different clinical manifestations of common pathological basis of reticuloendothelial proliferation Sexually transmitted diseases, collectively named as histiocytosis X. The clinical disease is relatively rare, only see the case report. Now our hospital from 1973 to 1989 admitted and confirmed by histopathology of orbital bone eosinophilic granuloma in 7 cases, on its clinical manifestations and treatment analysis and discussion.