Xavier Rogério Gastal, Silva Denise Rossato, Keiserman Mauro Waldemar, Lopes Maria Francisca Torres
Departamento de Medicina Interna, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil.
J Bras Pneumol. 2008 Dec;34(12):1074-8. doi: 10.1590/s1806-37132008001200014.
Kikuchi-Fujimoto disease is characterized by fever and lymphadenopathy, usually localized in the cervical region. This disease principally affects young females. It can be confused with lymphoma, adenocarcinoma metastasis and tuberculosis. We report two cases of Kikuchi-Fujimoto disease. In the first case, a 28-year-old female had been treated for tuberculosis one year prior and presented with a clinical and histological profile compatible with Kikuchi-Fujimoto disease. The second patient, a 58-year-old female, initially received treatment for Wegener's granulomatosis and, subsequently, for tuberculosis. Histopathological examination followed by immunohistochemical analysis confirmed the diagnosis of Kikuchi-Fujimoto disease in both cases. After the definitive diagnosis had been made, both patients were treated symptomatically, and both presented clinical improvement within one month. Subsequently, the latter patient developed systemic lupus erythematosus.
菊池-藤本病的特征为发热和淋巴结病,通常局限于颈部区域。这种疾病主要影响年轻女性。它可能与淋巴瘤、腺癌转移和结核病相混淆。我们报告两例菊池-藤本病。第一例中,一名28岁女性一年前曾接受结核病治疗,现表现出与菊池-藤本病相符的临床和组织学特征。第二例患者为一名58岁女性,最初接受韦格纳肉芽肿病治疗,随后接受结核病治疗。组织病理学检查及免疫组化分析确诊两例均为菊池-藤本病。确诊后,两名患者均接受了对症治疗,且均在一个月内临床症状改善。随后,后一名患者发展为系统性红斑狼疮。