David-Chaussé J, Dehais J, Picot C, Bullier R
Rev Rhum Mal Osteoartic. 1976 Feb;43(2):123-32.
The authors report the case of a 37-year-old man affected by a seronegative polyarthritis associated at first with erythroderma and then with cutaneous and subcutaneous papulo-nodular structures and a xanthomatous eryption. Histological examination of the cutaneous nodules and of the synovial membrane confirmed the diagnosis of multicentred reticulohistiocytosis by showing the presence of lipid infiltrates in the histiocyte cells and of multinucleate giant cells. A study of the ultrastructure of the histiocytes revealed the presence of numerous intracytoplasmic vacuoles. In spite of antimalaria treatment, with cortisone and then with immuno-depressants, the outcome was fatal with a picture of acute reticulosis and neurological disorders. In discussing this case, the authors also make a general review of the subject.
作者报告了一例37岁男性患者,其患有血清阴性多关节炎,起初伴有红皮病,随后出现皮肤和皮下丘疹结节结构以及黄瘤疹。对皮肤结节和滑膜进行组织学检查,通过显示组织细胞内存在脂质浸润和多核巨细胞,确诊为多中心网状组织细胞增生症。对组织细胞超微结构的研究揭示了大量胞质内空泡的存在。尽管采用了抗疟疾治疗,继以可的松然后是免疫抑制剂治疗,结局仍为致命,表现为急性网状细胞增多症和神经功能障碍。在讨论该病例时,作者还对该主题进行了全面综述。