Angioimmunoblastic lymphadenopathy followed by Kaposi's sarcoma.
Angioimmunoblastic lymphadenopathy followed by Kaposi's sarcoma.
复制标题
血管免疫母细胞性淋巴结病，随后是卡波西肉瘤。
DOI：
10.1001/archderm.1984.01650430148025
复制
发表时间：
1984
影响因子：
--
通讯作者：
C. Ramselaar
中科院分区：
文献类型：
--
作者：
H. Kluin;H. Elbers;C. Ramselaar
血管免疫母细胞性淋巴结病伴异常蛋白血症（AILD）是一种不常见的非肿瘤性淋巴组织增生性疾病。1进展为非霍奇金淋巴瘤的病例占10%-30%，但与其他恶性肿瘤相关的病例很少。1，2以前有3例AILD患者发生卡波西肉瘤。3 - 5在本文中，描述了第四个患者，在其中在一个淋巴结中发现了两种疾病的独特组合。病例报告：一位76岁的男性在入院前六周，双脚出现斑块和结节。在过去的几个月里，他经历了一阵阵发热伴全身瘙痒。在过去的一年里，他服用氨茶碱和盐酸多西环素治疗慢性支气管炎。体格检查发现坚固、可移动、无触痛的淋巴结，直径1 - 3 cm，可在下颌下触诊，
Angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) is an uncommon, nonneoplastic, lymphoproliferative disorder.1Progression into non-Hodgkin's lymphoma takes place in 10% to 30% of the cases, but an association with other malignant neoplasms occurs only rarely.1,2Previously the occurrence of Kaposi's sarcoma in patients with AILD has been described in three patients.3-5In this article, a fourth patient is described in whom the unique combination of both diseases was found in one lymph node. Report of a Case Plaques and nodules developed on both feet of a 76-year-old man six weeks before he was admitted to the hospital. During the previous months, he had experienced bouts of fever with generalized pruritus. For the past year he had taken aminophylline and doxycycline hydrochloride for chronic bronchitis. Physical examination disclosed firm, movable, nontender lymph nodes, ranging in size from 1 to 3 cm in diameter, that were palpated in the submandibular,