Varadachari C, Palutke M, Climie A R, Weise R W, Chason J L
J Neurosurg. 1978 Dec;49(6):887-92. doi: 10.3171/jns.1978.49.6.0887.
A group of central nervous system neoplasms, previously known as reticulum cell sarcoma or microglioma, and recently classified as malignant lymphoma, histiocytic type, not infrequently occur in patients with immunodeficiency, either primary or induced by immunosuppressant drugs. The authors report such a neoplasm in a patient with idiopathic thrombocytopenic purpura immunosuppressed with azathioprine and prednisone. The neoplasm was studied with several immunological techniques and by electron microscopy. The neoplasm had B lymphocyte membrane markers and showed plasmacytic differentiation. These features suggest that it was a tumor of transformed B lymphocytes (immunoblasts).
一组中枢神经系统肿瘤,以前称为网状细胞肉瘤或小胶质细胞瘤,最近被归类为组织细胞型恶性淋巴瘤,在原发性免疫缺陷患者或由免疫抑制药物引起的免疫缺陷患者中并不罕见。作者报告了一名患有特发性血小板减少性紫癜并接受硫唑嘌呤和泼尼松免疫抑制治疗的患者发生了此类肿瘤。采用多种免疫技术和电子显微镜对该肿瘤进行了研究。该肿瘤具有B淋巴细胞膜标志物并显示浆细胞分化。这些特征表明它是一种转化B淋巴细胞(免疫母细胞)的肿瘤。