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目的：探讨肠型恶性组织细胞病（恶组）临床特征及确诊方法。方法：对８例肠型恶组的临床资料进行回顾性分析。结果：肠型恶组的临床症状复杂多样，其表现主要集中在肠道。反复骨髓穿刺尤其在骨痛明显处取材为确诊的主要手段，联合化疗可延长生存期。结论：肠型恶组较罕见，怀疑本病时应及早反复骨髓穿刺等检查，尽快确诊，争取治疗时机，以减少误诊、误治。
Objective: To investigate the clinical features and diagnosis methods of intestinal malignant histiocytosis (evil group). Methods: Retrospective analysis was performed on the clinical data of 8 cases of bowel type. RESULTS: The clinical symptoms of the intestinal-type group were complex and varied, and their performance was mainly concentrated in the intestinal tract. Repeated bone marrow puncture, especially in the apparent bone pain as the main means of diagnosis, combined with chemotherapy can prolong survival. Conclusion: Intestinal type evil group is relatively rare. When the disease is suspected, bone marrow puncture and other tests should be repeated as soon as possible to confirm the diagnosis as soon as possible. The timing of treatment should be strived to reduce misdiagnosis and mistreatment.