Nagler A, Ben-Arieh Y, Brenner B, Tatarsky I, Pollack S
Am J Hematol. 1986 Nov;23(3):277-81. doi: 10.1002/ajh.2830230312.
We describe a 63-year-old male patient with severe osteoporosis, multiple lytic bone lesions, and monoclonal gammopathy (IgG lambda). Whereas the tentative diagnosis in this case was multiple myeloma, bone marrow trephine biopsies of the iliac crest and from an osteolytic lesion of the tibia both showed a peculiar infiltrate consisting of numerous elongated mast cells, eosinophils, and some plasma cells and lymphocytes. The bone marrow lesions fit the diagnosis of eosinophilic fibrohistiocytic lesion of bone marrow (EFHBM). The patient had no abnormality that could be related to a known allergic disease, and no relationship to drug hypersensitivity could be established. The features of the bone marrow infiltrate and its association with monoclonal gammopathy may suggest a linkage between EFHBM and the monoclonal gammopathy.
我们描述了一名63岁男性患者,患有严重骨质疏松症、多发溶骨性骨病变和单克隆丙种球蛋白病(IgG λ)。尽管该病例的初步诊断为多发性骨髓瘤,但髂嵴和胫骨溶骨性病变的骨髓环钻活检均显示出一种特殊的浸润,由大量细长的肥大细胞、嗜酸性粒细胞以及一些浆细胞和淋巴细胞组成。骨髓病变符合骨髓嗜酸性纤维组织细胞性病变(EFHBM)的诊断。该患者没有可归因于已知过敏性疾病的异常情况,也无法确定与药物超敏反应的关系。骨髓浸润的特征及其与单克隆丙种球蛋白病的关联可能提示EFHBM与单克隆丙种球蛋白病之间存在联系。