Friedman-Birnbaum R, Gilhar A, Carter A
J Dermatol Surg Oncol. 1985 Jan;11(1):76-9. doi: 10.1111/j.1524-4725.1985.tb02894.x.
A 66-year-old woman who developed simultaneously angioimmunoblastic lymphadenopathy (AILD) and Kaposi's sarcoma (KS) is reported. A parallel course of the two diseases was evident. After a relatively short course of corticosteroid therapy, the clinical and laboratory signs of AILD regressed, and the patient is in remission 39 months after the beginning of the disease. At the same time a regression of KS lesions was also observed. The frequent association of KS and lymphoproliferative disorders in the same patient is discussed. As AILD is a lymphoma-like syndrome, it is suggested that we might expect a more frequent association of this disease with KS in the same patient than the two cases reported to date.
报告了一名66岁女性，她同时发生血管免疫母细胞性淋巴结病（AILD）和卡波西肉瘤（KS）。两种疾病呈平行病程。经过相对短期的皮质类固醇治疗，AILD的临床和实验室体征消退，患者在疾病开始后39个月处于缓解期。同时也观察到KS病变的消退。讨论了同一患者中KS与淋巴增殖性疾病的频繁关联。由于AILD是一种淋巴瘤样综合征，因此提示我们可能会预期在同一患者中这种疾病与KS的关联比迄今报道的两例更为频繁。
