A Case of Methimazole-induced Agranulocytosis and Kikuchi's Disease in a Patient with Graves' Disease

Seung Eun Lee, Jihyun Ahn, Jaetaek Kim, Yeon-sahng Oh, Y. Chung
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Abstract

Methimazole-induced agranulocytosis is a rare, but critical side effect that should be recognized as soon as possible since it may induce a life-threatening condition when it was overlooked. Histiocytic necrotizing lymphadenitis is also called Kikuchi’s lymphadenitis, and this is a rare form of lymphadenitis with a self-limited clinical course and this illness is accompanied by cervical lymph node enlargement, fever and malaise. We recently experienced a patient with methimazole-induced agranulocytosis and Graves' disease, and this was accompanied by Kikuchi's disease; the patient presented with sore throat and multiple enlarged cervical lymph nodes. To the best of our knowledge, there is no previous report on methimazole-induced agranulocytosis combined with Kikuchi's disease. Therefore, we report here on this very rare case along with a brief review of the relevant literature. (J Korean Endocr Soc 23:420~424, 2008) ꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏ
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甲巯咪唑致格雷夫斯病患者粒细胞缺乏症和菊池病1例
甲巯咪唑诱导的粒细胞缺乏症是一种罕见但严重的副作用,应尽早发现,因为如果忽视它可能会导致危及生命的疾病。组织细胞坏死性淋巴结炎也被称为菊池淋巴结炎,这是一种罕见的淋巴结炎,具有自限性的临床病程,这种疾病伴随着颈部淋巴结肿大,发烧和不适。我们最近遇到了一位甲巯咪唑诱导的粒细胞缺乏症和Graves病的患者,并伴有菊池病;患者表现为喉咙痛及颈部多发肿大淋巴结。据我们所知,以前没有甲巯咪唑诱导的粒细胞缺乏症合并菊池病的报道。因此,我们在此报告这个非常罕见的病例,并简要回顾相关文献。(J韩国Endocr Soc 23:420 ~ 424, 2008)ꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏꠏ
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