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Unusual and rare case of generalised lymphadenopathy: Kimura’s disease

机译:普通淋巴结病的不寻常和罕见的情况:Kimura病

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摘要

We report a case of Kimura’s disease in a 65-year-old woman who presented with generalised itching, abdominal pain, facial puffiness, difficulty in swallowing and loss of appetite. She was found to have generalised lymphadenopathy and a fine-needle aspiration cytology initially done revealed ‘reactive lymphadenitis’ which was inconclusive. PET-CT done showed features suggestive of lymphoma. Hence, lymph node biopsy was done for confirmation and incidentally after immunohistochemistry staining it turned out to be Kimura’s disease. High-dose steroid therapy was started and patient showed dramatic clinical and symptomatic improvement. Kimura’s disease almost always presents as cervical lymphadenopathy and usually never causes compressive symptoms. Our patient presented with compressive symptoms and generalised lymphadenopathy which is a rarity.
机译:我们在一名65岁的女性中举报了一个患有广义瘙痒,腹痛,面部浮肿,难以吞咽和失去食欲的困难的情况。她被发现具有广泛的淋巴结病,最初进行了细针抽吸细胞学,揭示了“活性淋巴结炎”,这是不确定的。 PET-CT完成表明淋巴瘤的暗示功能。因此,淋巴结活检是为了确认,并且在免疫组织化学染色后偶然是Kimura疾病。开始高剂量类固醇疗法,患者表现出显着的临床和症状性改善。 Kimura的疾病几乎总是作为宫颈淋巴结病,通常永远不会导致压缩症状。我们的病人患有压缩症状和广义淋巴结病,这是一种罕见。

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