Jacobson R J, Schmaman A, Morley J E, Golding B, Rippey J J
S Afr Med J. 1976 Apr 24;50(18):707-10.
Angio-immunoblastic lymphadenopathy (AILD) was diagnosed in 3 Black patients, AILD is a non-malignant disorder which resembles a malignant lymphoma clinically and morphologically. It is thought to represent an abnormal response of B lymphocytes to antigenic stimuli which are often therapeutic agents. The disorder usually affects adults of the older age group and the clinical course can be rapidly fatal, particularly if vigorous chemotherapy is given. Of the 3 patients with AILD, 2 died from complicating infections within 6 months after the initial diagnosis. The third patient was completely cured after short courses of prednisone and vincristine. It appears that in some patients the disorder may be completely reversible but whether these patients are at a greater risk of eventually developing a lymphoma is uncertain at the present time, and remains to be ascertained by their long-term follow-up.
3名黑人患者被诊断为血管免疫母细胞性淋巴结病(AILD)。AILD是一种非恶性疾病,在临床和形态学上类似于恶性淋巴瘤。它被认为代表B淋巴细胞对抗原刺激(通常是治疗药物)的异常反应。该疾病通常影响老年人群体中的成年人,临床病程可能迅速致命,特别是在进行积极化疗的情况下。在3名AILD患者中,2例在初诊后6个月内死于并发感染。第3例患者在短期使用泼尼松和长春新碱后完全治愈。似乎在某些患者中,该疾病可能完全可逆,但目前尚不确定这些患者最终发生淋巴瘤的风险是否更高,仍有待通过长期随访来确定。