美国文献中此病被称为免疫母细胞淋巴腺病(IBL)或血管免疫母细胞淋巴腺病伴异常蛋白血症(AILD),Kiel淋巴瘤组称它为淋巴肉芽肿病X(LgX).组织病理学定义AILD、IBL和LgX的组织学诊断依据的主要表现是一致的,即淋巴结结构被涂抹、血管增生和多样性的细胞学.但三者的附加表现不同,IBL的诊断还需有淋巴细胞消减和间质中PAS阳性物质,以及无残存滤泡的表现.LgX则包括一组淋巴细胞为主 In the United States, the disease is called immunoblastic lymphadenopathy (IBL) or angioimmunoblastic lymphadenopathy with an anaphylactoid protein (AILD), which the Kiel Lymphoma Group calls Lympho-granulomatosis X (LgX). Histopathology Definition The histological basis for diagnosis of AILD, IBL and LgX is consistent with the main findings that the lymph node structure is smeared, vascular hyperplasia and diversity of cytology, but the three additional manifestations of different IBL diagnosis also need to have Lymphocyte depletion and interstitial PAS-positive substances, as well as the performance of no residual follicles.LgX includes a group of lymphocyte-based