KIKUCHI-FUJIMOTO DISEASE IN A 24-YEARS OLD SAUDI FEMALE IN SAUDI ARABIA

A. Ashour, M. Albeshri, H. Marzouki, S. Al-Khayyat
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Abstract

Kikuchi-Fujimoto disease (KFD) is a very rare, self-limited and benign inflammatory disorder. It was first reported in Japan in 1972. Diagnosis of Kikuchi disease is confirmed by histopathological investigation of lymph node (LN) biopsy under ultrasound guidance. Computed tomography (CT) and magnetic resonance imaging (MRI) help in diagnosis of Kikuchi cervical lymphadenopathy but don’t provide a definitive diagnosis. We describe a case of KFD affecting the cervical lymph nodes of a 24-year old Saudi female.
沙特阿拉伯一名24岁沙特女性的菊chi - fujimoto病
菊chi- fujimoto病(KFD)是一种非常罕见的、自限性的良性炎症性疾病。1972年,日本首次报道了这种疾病。菊池病的诊断是通过超声引导下淋巴结活检的组织病理学检查来证实的。计算机断层扫描(CT)和磁共振成像(MRI)有助于诊断菊池颈部淋巴结病,但不能提供明确的诊断。我们描述了一个病例KFD影响颈部淋巴结的一个24岁的沙特女性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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