Bernstein J E, Soltani K, Lorincz A L
J Am Acad Dermatol. 1979 Sep;1(3):227-32. doi: 10.1016/s0190-9622(79)70014-4.
Angioimmunoblastic lymphadenopathy (AIL) is an uncommon immunoproliferative disorder with a presentation similar to malignant lymphoma but with a benign histopathologic picture. We report a case of a 49-year-old woman with AIL who manifested a pruritic maculopapular eruption as her presenting complaint and whose disease pursued an aggressive clinical course. Forty-four percent of patients with AIL experience a nonspecific dermatitis that in general is maculopapular and precedes other clinical symptoms by at least several weeks. AIL should be included in the differential diagnosis of any maculopapular eruption of unknown etiology accompanied by lymphadenopathy.
血管免疫母细胞性淋巴结病（AIL）是一种罕见的免疫增殖性疾病，临床表现类似于恶性淋巴瘤，但组织病理学表现为良性。我们报告一例49岁患有AIL的女性病例，该患者以瘙痒性斑丘疹为首发症状，其病情呈侵袭性临床过程。44%的AIL患者会出现非特异性皮炎，通常为斑丘疹，且比其他临床症状至少提前几周出现。对于任何病因不明且伴有淋巴结病的斑丘疹，AIL都应列入鉴别诊断范围。
