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本文对我院二十一年来收治的组织细胞增生症X33例做了分析总结。提出了一组无皮肤损害,无三联症等特点、而以淋巴结及肝脾大为主要表现的高分化组织细胞增生症。从其经过缓慢、予后较好,无明显造血障碍等方面可与其它恶性组织细胞增生病鉴别,但是否与本组疾病同属一类、值得商讨。另外还报告两例家族性病例,两例有精神症状及1例出现颅神经瘫痪的病例,但因例数不多,资料也不够完善,尚须今后进一步探讨。
In this paper, our hospital for twenty-one years admitted to histiocytosis X33 cases were analyzed and summarized. Proposed a group of no skin damage, no triad symptoms, and other characteristics of the lymph nodes and liver and spleen as the main manifestation of well-differentiated histiocytosis. It can be differentiated from other malignant tissue cell proliferations from its slow, better prognosis, no obvious hematopoietic disorders, but it is worth discussing whether it is in the same category as the diseases of this group. In addition, two cases of familial cases were also reported. Two cases had psychiatric symptoms and one case had cranial nerve paralysis. However, due to a small number of cases, the data were not perfect enough and should be further explored in the future.