Said J W
Department of Pathology, Cedars Sinai Medical Center, Los Angeles, CA 90048.
Semin Diagn Pathol. 1988 Nov;5(4):365-75.
Lymphoid proliferations in the acquired immunodeficiency syndrome reflect the profound immunologic imbalances induced by the lymphotropic human immunodeficiency virus, and comprise a range of lymphoproliferative disorders from benign lymphadenopathy to malignant lymphoma. Persistent generalized lymphadenopathy (PGL) is associated with a frequently debilitating complex of clinical symptoms and waxing and waning lymphadenopathy. Biopsies of lymph nodes, bone marrow, and other involved tissues show a spectrum of abnormal lymphoid proliferations, with eventual lymphoid depletion, lymphadenopathic Kaposi's sarcoma, and malignant lymphoma. Although individual features of AIDS-related lymphadenopathy may not be specific, the constellation of histologic, immunologic, and ultrastructural findings is highly characteristic of the disorder and useful as a predictor of clinical course. Malignant lymphomas that develop within this setting of multicloncal B cell expansion and impaired immune surveillance have distinctive clinical, histologic, and molecular biologic parameters.
获得性免疫缺陷综合征中的淋巴组织增生反映了嗜淋巴细胞性人类免疫缺陷病毒引起的严重免疫失衡,包括从良性淋巴结病到恶性淋巴瘤的一系列淋巴组织增生性疾病。持续性全身性淋巴结病(PGL)与一组常常使人衰弱的临床症状以及时起时伏的淋巴结病相关。淋巴结、骨髓及其他受累组织的活检显示一系列异常的淋巴组织增生,最终出现淋巴细胞耗竭、淋巴结病性卡波西肉瘤和恶性淋巴瘤。尽管艾滋病相关淋巴结病的个别特征可能不具有特异性,但组织学、免疫学和超微结构检查结果的组合对该疾病具有高度特征性,且有助于预测临床病程。在这种多克隆B细胞扩增和免疫监视受损的背景下发生的恶性淋巴瘤具有独特的临床、组织学和分子生物学特征。