Limpert J, MacMahon H, Variakojis D
Radiology. 1984 Jul;152(1):27-30. doi: 10.1148/radiology.152.1.6729133.
The authors describe the clinical and radiographic features in 7 patients with angioimmunoblastic lymphadenopathy (AIL) with dysproteinemia. This condition should be considered in any patient over 50 who presents with constitutional symptoms such as fever, weight loss, and malaise accompanied by involvement of the peripheral and hilar or mediastinal lymph nodes. Contrary to previous reports, the anterior mediastinal nodes may be involved. Intrapulmonary masses accompanied by clinical deterioration may indicate transformation to immunoblastic lymphoma. The gallium scans and radiographic appearance assist in the diagnosis, but lymph node biopsy is necessary in order to distinguish AIL from lymphoma.
作者描述了7例伴有蛋白异常血症的血管免疫母细胞性淋巴结病(AIL)患者的临床和影像学特征。对于任何50岁以上出现发热、体重减轻和不适等全身症状并伴有外周及肺门或纵隔淋巴结受累的患者,均应考虑此病。与既往报道相反,前纵隔淋巴结可能受累。伴有临床病情恶化的肺内肿块可能提示已转变为免疫母细胞性淋巴瘤。镓扫描和影像学表现有助于诊断,但为了将AIL与淋巴瘤区分开来,淋巴结活检是必要的。