Kikuchi disease: An unusual cause of cervical lymphadenopathy in a young female

Vidyulata Madhu, R. Sreedharan, V. Vinukumar
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Abstract

Kikuchi-Fujimoto disease (KD), also known as histiocytic necrotizing lymphadenitis, is a rare cause of unilateral cervical lymphadenopathy usually described in adolescents and young adults with female preponderance. Clinically patients present with palpable lymphadenopathy, fever, and loss of weight. Hence, it should be differentiated from other causes of lymphadenopathy such as tuberculosis, lymphoma, or malignancy. Although the majority resolve spontaneously without treatment some may require non-steroidal anti-inflammatory drug or steroids. It may also be associated with systemic lupus erythematosus. Hence early detection, prompt diagnosis, and follow-up of the patient are essential in all cases of unilateral cervical lymphadenopathy in young adults. Here, we describe a 22-year old female who presented with unilateral neck swelling and was clinically diagnosed initially as a case of tuberculous lymphadenitis which on biopsy turned out to be KD.
菊池病:年轻女性颈部淋巴结病的一种罕见病因
Kikuchi-Fujimoto病(KD),也被称为组织细胞坏死性淋巴结炎,是一种罕见的单侧颈部淋巴结病,通常发生在青少年和年轻成人中,以女性为主。临床表现为可触及的淋巴结病、发热和体重减轻。因此,它应与其他原因的淋巴结病如结核、淋巴瘤或恶性肿瘤区分开来。虽然大多数不需治疗自行消退,但有些可能需要非甾体抗炎药或类固醇。它也可能与系统性红斑狼疮有关。因此,早期发现,及时诊断,并随访患者是必要的,在所有情况下单侧颈淋巴肿大的年轻人。在这里,我们描述了一位22岁的女性,她表现为单侧颈部肿胀,最初被临床诊断为结核性淋巴结炎,活检结果为KD。
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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