一个小男孩的泛性淋巴瘤病:一种罕见的基库奇 - 藤本病
Anand Nandkumar Dugad1, Vivek Hitesh Lapsiwala
1Department of General Medicine, Dr. D.Y. Patil Vidyapeeth, Pune, Maharashtra, India.
Annals of African medicine
|August 20, 2025
概括
在男孩中,Kikuchi-Fujimoto疾病 (KFD) 是罕见的. 这份病例报告详细介绍了一名15岁的男性, 在诊断延迟3年后被诊断患有KFD,
科学领域:
- 儿童病理学
- 免疫学
- 罕见疾病
背景情况:
- 基库奇-富士莫托病 (KFD) 或囊性瘤性淋巴腺炎是一种罕见的良性疾病.
- 癌症通常影响年轻女性,在儿童和男性中不常见.
研究的目的:
- 报告一个15岁男孩患有KFD的病例,
- 突出诊断的挑战和基因病理在KFD的重要性.
主要方法:
- 一个15岁的男性患有淋巴腺综合症.
- 最初的细针吸血细胞学和淋巴结活检.
- 最终的诊断证实了下淋巴结组织病理学显示死淋巴结炎.
主要成果:
- 一名15岁的男孩出现了泛性淋巴腺病,发烧和疼痛.
- 经过3年的初始活检显示出反应性/急性淋巴腺炎,延迟了KFD的诊断.
- 组织病理学证实了基库奇病 (没有颗粒瘤的瘤性淋巴炎).
结论:
- 在像青少年男性这样的非典型人群中,诊断KFD可能具有挑战性.
- 持续或复发的淋巴腺病症需要进行重复的组织病理学评估以确切诊断.
- 用NSAID和抗生素治疗患者的症状有所改善.
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