Tosi P, Auteri A, Cintorino M, Pasini F L, Luzi P
Tumori. 1979 Jun 30;65(3):363-71. doi: 10.1177/030089167906500313.
A case of clinically and morphologically typical angioimmunoblastic lymphadenopathy (AILD) in a 68-year-old man during a prolonged antibiotic treatment for urinary infection is presented. Lymph node biopsy at first showed findings suggestive of an exhaustion of the germinal center immunological activity (like those characterizing angiofollicular lymph any clear transition into malignant lymphoma. The course of the disease was characterized by the occurrence of opportunistic infections (toxoplasmosis, herpes zoster), and finally by the onset of a cutaneous Kaposi's sarcoma. The possible relation of AILD to Kaposi's sarcoma is discussed, and the main clinical and morphological data of the case of AILD (about 200) reported in the literature are reviewed.
本文报告了一例68岁男性在长期抗生素治疗尿路感染期间发生的临床和形态学典型的血管免疫母细胞性淋巴结病（AILD）。最初的淋巴结活检结果提示生发中心免疫活性耗竭（类似于血管滤泡性淋巴瘤的特征），但未发现向恶性淋巴瘤的明确转变。该疾病的病程特点是发生机会性感染（弓形虫病、带状疱疹），最终出现皮肤卡波西肉瘤。讨论了AILD与卡波西肉瘤的可能关系，并回顾了文献中报道的AILD病例（约200例）的主要临床和形态学数据。
